Canonical Allele Identifier: CA2742038374

Gene: BDNF BDNF-AS

Linked Data

• ClinVar Variation Id: 3024130
• ClinVar RCV Id: RCV003881714

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.[27656036C>A;27658369C>T;27672694G>C] , CM000673.2:g.[27656036C>A;27658369C>T;27672694G>C]	GRCh38
NC_000011.9:g.[27677583C>A;27679916C>T;27694241G>C] , CM000673.1:g.[27677583C>A;27679916C>T;27694241G>C]	GRCh37
NC_000011.8:g.[27634159C>A;27636492C>T;27650817G>C]	NCBI36
NG_011794.1:g.[54365C>G;68690G>A;71022G>T]

Transcript Alleles

HGVS	Amino-acid change
ENST00000356660.9:c.[-21-14109C>G;196G>A;*1785G>T] (BDNF) MANE Select	ENSP00000349084.4:[p.Val66Met;n.196G>A]
ENST00000314915.6:c.[4-14109C>G;220G>A;*1785G>T] (BDNF)	ENSP00000320002.6:[p.Val74Met;n.220G>A]
ENST00000356660.8:c.[-21-14109C>G;196G>A;*1785G>T] (BDNF)	ENSP00000349084.4:[p.Val66Met;n.196G>A]
ENST00000395978.7:c.[-21-14109C>G;196G>A;*1785G>T] (BDNF)	ENSP00000379302.3:[p.Val66Met;n.196G>A]
ENST00000395980.6:c.[-21-14109C>G;196G>A;*1785G>T] (BDNF)	ENSP00000379304.2:[p.Val66Met;n.196G>A]
ENST00000395981.7:c.[-21-14109C>G;196G>A;*1785G>T] (BDNF)	ENSP00000379305.3:[p.Val66Met;n.196G>A]
ENST00000395983.7:c.[-21-14109C>G;196G>A;*1785G>T] (BDNF)	ENSP00000379307.3:[p.Val66Met;n.196G>A]
ENST00000395986.6:c.[25-14109C>G;241G>A;*1785G>T] (BDNF)	ENSP00000379309.2:[p.Val81Met;n.241G>A]
ENST00000418212.5:c.[-128-13768C>G;196G>A;*1785G>T] (BDNF)	ENSP00000400502.1:[p.Val66Met;n.196G>A]
ENST00000420794.2:c.[-139+1366C>G;196G>A;*1785G>T] (BDNF)	ENSP00000389564.1:[p.Val66Met;n.196G>A]
ENST00000438929.5:c.[225+1366C>G;442G>A;*1785G>T] (BDNF)	ENSP00000414303.1:[p.Val148Met;n.442G>A]
ENST00000525950.5:c.[-21-14109C>G;196G>A;*1785G>T] (BDNF)	ENSP00000432035.1:[p.Val66Met;n.196G>A]
ENST00000530786.5:c.[225+1366C>G;*325G>A;*2658G>T] (BDNF)	ENSP00000433003.1:n.[225+1366C>G;*325G>A;...
ENST00000530861.5:c.[-21-14109C>G;196G>A;*1785G>T] (BDNF)	ENSP00000435564.1:[p.Val66Met;n.196G>A]
ENST00000532997.5:c.[-21-14109C>G;196G>A;*1785G>T] (BDNF)	ENSP00000435805.1:[p.Val66Met;n.196G>A]
ENST00000533131.5:c.[-21-14109C>G;196G>A;*1785G>T] (BDNF)	ENSP00000432727.1:[p.Val66Met;n.196G>A]
ENST00000533246.5:c.[-21-14109C>G;196G>A;*1785G>T] (BDNF)	ENSP00000432376.1:[p.Val66Met;n.196G>A]
ENST00000584049.5:n.[338-14109C>G;554G>A;2887G>T] (BDNF)
NM_001143805.1:c.[-21-14109C>G;196G>A;*1784G>T] (BDNF)	NP_001137277.1:[p.Val66Met;n.196G>A]
NM_001143806.1:c.[-21-14109C>G;196G>A;*1784G>T] (BDNF)	NP_001137278.1:[p.Val66Met;n.196G>A]
NM_001143807.1:c.[-21-14109C>G;196G>A;*1784G>T] (BDNF)	NP_001137279.1:[p.Val66Met;n.196G>A]
NM_001143808.1:c.[-21-14109C>G;196G>A;*1784G>T] (BDNF)	NP_001137280.1:[p.Val66Met;n.196G>A]
NM_001143809.1:c.[67-14109C>G;283G>A;*1784G>T] (BDNF)	NP_001137281.1:[p.Val95Met;n.283G>A]
NM_001143810.1:c.[225+1366C>G;442G>A;*1784G>T] (BDNF)	NP_001137282.1:[p.Val148Met;n.442G>A]
NM_001143811.1:c.[-139+1366C>G;196G>A;*1784G>T] (BDNF)	NP_001137283.1:[p.Val66Met;n.196G>A]
NM_001143812.1:c.[-21-14109C>G;196G>A;*1784G>T] (BDNF)	NP_001137284.1:[p.Val66Met;n.196G>A]
NM_001143813.1:c.[-21-14109C>G;196G>A;*1784G>T] (BDNF)	NP_001137285.1:[p.Val66Met;n.196G>A]
NM_001143814.1:c.[-128-13768C>G;196G>A;*1784G>T] (BDNF)	NP_001137286.1:[p.Val66Met;n.196G>A]
NM_001709.4:c.[-21-14109C>G;196G>A;*1784G>T] (BDNF)	NP_001700.2:[p.Val66Met;n.196G>A]
NM_170731.4:c.[4-14109C>G;220G>A;*1784G>T] (BDNF)	NP_733927.1:[p.Val74Met;n.220G>A]
NM_170732.4:c.[-21-14109C>G;196G>A;*1784G>T] (BDNF)	NP_733928.1:[p.Val66Met;n.196G>A]
NM_170733.3:c.[-21-14109C>G;196G>A;*1784G>T] (BDNF)	NP_733929.1:[p.Val66Met;n.196G>A]
NM_170734.3:c.[25-14109C>G;241G>A;*1784G>T] (BDNF)	NP_733930.1:[p.Val81Met;n.241G>A]
NR_002832.2:n.[375-2205C>A;503C>T;655-2603G>C] (BDNF-AS)
NR_033312.1:n.[306-2205C>A;434C>T;586-2883G>C] (BDNF-AS)
NR_033313.1:n.[306-2205C>A;434C>T;585+13466G>C] (BDNF-AS)
NR_033314.1:n.[375-2205C>A;503C>T;655-4288G>C] (BDNF-AS)
NR_033315.1:n.[306-2205C>A;434C>T;586-4288G>C] (BDNF-AS)
XM_011520280.1:c.[225+1366C>G;442G>A;*1785G>T] (BDNF)	XP_011518582.1:[p.Val148Met;n.442G>A]
XM_011520280.2:c.[225+1366C>G;442G>A;*1785G>T] (BDNF)	XP_011518582.1:[p.Val148Met;n.442G>A]
NM_001709.5:c.[-21-14109C>G;196G>A;*1785G>T] (BDNF) MANE Select	NP_001700.2:[p.Val66Met;n.196G>A]
NM_001143807.2:c.[-21-14109C>G;196G>A;*1785G>T] (BDNF)	NP_001137279.1:[p.Val66Met;n.196G>A]
NM_001143813.2:c.[-21-14109C>G;196G>A;*1785G>T] (BDNF)	NP_001137285.1:[p.Val66Met;n.196G>A]
NM_001143814.2:c.[-128-13768C>G;196G>A;*1785G>T] (BDNF)	NP_001137286.1:[p.Val66Met;n.196G>A]
NM_170731.5:c.[4-14109C>G;220G>A;*1785G>T] (BDNF)	NP_733927.1:[p.Val74Met;n.220G>A]
NM_001143808.2:c.[-21-14109C>G;196G>A;*1785G>T] (BDNF)	NP_001137280.1:[p.Val66Met;n.196G>A]
NM_001143809.2:c.[67-14109C>G;283G>A;*1785G>T] (BDNF)	NP_001137281.1:[p.Val95Met;n.283G>A]
NM_001143810.2:c.[225+1366C>G;442G>A;*1785G>T] (BDNF)	NP_001137282.1:[p.Val148Met;n.442G>A]
NM_001143811.2:c.[-139+1366C>G;196G>A;*1785G>T] (BDNF)	NP_001137283.1:[p.Val66Met;n.196G>A]
NM_001143812.2:c.[-21-14109C>G;196G>A;*1785G>T] (BDNF)	NP_001137284.1:[p.Val66Met;n.196G>A]
NM_170733.4:c.[-21-14109C>G;196G>A;*1785G>T] (BDNF)	NP_733929.1:[p.Val66Met;n.196G>A]
NM_170734.4:c.[25-14109C>G;241G>A;*1785G>T] (BDNF)	NP_733930.1:[p.Val81Met;n.241G>A]