Canonical Allele Identifier: CA219852069

Gene: BDNF BDNF-AS

Linked Data

• dbSNP Id: rs766339291
• gnomAD v4: 11-27658207-C-T
• MyVariant Identifiers: chr11:g.27679754C>T (hg19) ; chr11:g.27658207C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.27658207C>T , CM000673.2:g.27658207C>T	GRCh38
NC_000011.9:g.27679754C>T , CM000673.1:g.27679754C>T	GRCh37
NC_000011.8:g.27636330C>T	NCBI36
NG_011794.1:g.68852G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356660.9:c.358G>A (BDNF) MANE Select	ENSP00000349084.4:p.Ala120Thr
ENST00000314915.6:c.382G>A (BDNF)	ENSP00000320002.6:p.Ala128Thr
ENST00000356660.8:c.358G>A (BDNF)	ENSP00000349084.4:p.Ala120Thr
ENST00000395978.7:c.358G>A (BDNF)	ENSP00000379302.3:p.Ala120Thr
ENST00000395980.6:c.358G>A (BDNF)	ENSP00000379304.2:p.Ala120Thr
ENST00000395981.7:c.358G>A (BDNF)	ENSP00000379305.3:p.Ala120Thr
ENST00000395983.7:c.358G>A (BDNF)	ENSP00000379307.3:p.Ala120Thr
ENST00000395986.6:c.403G>A (BDNF)	ENSP00000379309.2:p.Ala135Thr
ENST00000418212.5:c.358G>A (BDNF)	ENSP00000400502.1:p.Ala120Thr
ENST00000420794.2:c.358G>A (BDNF)	ENSP00000389564.1:p.Ala120Thr
ENST00000438929.5:c.604G>A (BDNF)	ENSP00000414303.1:p.Ala202Thr
ENST00000439476.6:c.358G>A (BDNF)	ENSP00000389345.2:p.Ala120Thr
ENST00000525528.1:c.358G>A (BDNF)	ENSP00000437138.1:p.Ala120Thr
ENST00000525950.5:c.358G>A (BDNF)	ENSP00000432035.1:p.Ala120Thr
ENST00000530786.5:c.*487G>A (BDNF)	ENSP00000433003.1:n.*487G>A
ENST00000530861.5:c.358G>A (BDNF)	ENSP00000435564.1:p.Ala120Thr
ENST00000532997.5:c.358G>A (BDNF)	ENSP00000435805.1:p.Ala120Thr
ENST00000533131.5:c.358G>A (BDNF)	ENSP00000432727.1:p.Ala120Thr
ENST00000533246.5:c.358G>A (BDNF)	ENSP00000432376.1:p.Ala120Thr
ENST00000584049.5:n.716G>A (BDNF)
NM_001143805.1:c.358G>A (BDNF)	NP_001137277.1:p.Ala120Thr
NM_001143806.1:c.358G>A (BDNF)	NP_001137278.1:p.Ala120Thr
NM_001143807.1:c.358G>A (BDNF)	NP_001137279.1:p.Ala120Thr
NM_001143808.1:c.358G>A (BDNF)	NP_001137280.1:p.Ala120Thr
NM_001143809.1:c.445G>A (BDNF)	NP_001137281.1:p.Ala149Thr
NM_001143810.1:c.604G>A (BDNF)	NP_001137282.1:p.Ala202Thr
NM_001143811.1:c.358G>A (BDNF)	NP_001137283.1:p.Ala120Thr
NM_001143812.1:c.358G>A (BDNF)	NP_001137284.1:p.Ala120Thr
NM_001143813.1:c.358G>A (BDNF)	NP_001137285.1:p.Ala120Thr
NM_001143814.1:c.358G>A (BDNF)	NP_001137286.1:p.Ala120Thr
NM_001143816.1:c.358G>A (BDNF)	NP_001137288.1:p.Ala120Thr
NM_001709.4:c.358G>A (BDNF)	NP_001700.2:p.Ala120Thr
NM_170731.4:c.382G>A (BDNF)	NP_733927.1:p.Ala128Thr
NM_170732.4:c.358G>A (BDNF)	NP_733928.1:p.Ala120Thr
NM_170733.3:c.358G>A (BDNF)	NP_733929.1:p.Ala120Thr
NM_170734.3:c.403G>A (BDNF)	NP_733930.1:p.Ala135Thr
NM_170735.5:c.358G>A (BDNF)	NP_733931.1:p.Ala120Thr
NR_002832.2:n.375-34C>T (BDNF-AS)
NR_033312.1:n.306-34C>T (BDNF-AS)
NR_033313.1:n.306-34C>T (BDNF-AS)
NR_033314.1:n.375-34C>T (BDNF-AS)
NR_033315.1:n.306-34C>T (BDNF-AS)
XM_011520280.1:c.604G>A (BDNF)	XP_011518582.1:p.Ala202Thr
XM_011520280.2:c.604G>A (BDNF)	XP_011518582.1:p.Ala202Thr
NM_001709.5:c.358G>A (BDNF) MANE Select	NP_001700.2:p.Ala120Thr
NM_001143807.2:c.358G>A (BDNF)	NP_001137279.1:p.Ala120Thr
NM_001143813.2:c.358G>A (BDNF)	NP_001137285.1:p.Ala120Thr
NM_001143814.2:c.358G>A (BDNF)	NP_001137286.1:p.Ala120Thr
NM_170731.5:c.382G>A (BDNF)	NP_733927.1:p.Ala128Thr
NM_001143808.2:c.358G>A (BDNF)	NP_001137280.1:p.Ala120Thr
NM_001143809.2:c.445G>A (BDNF)	NP_001137281.1:p.Ala149Thr
NM_001143810.2:c.604G>A (BDNF)	NP_001137282.1:p.Ala202Thr
NM_001143811.2:c.358G>A (BDNF)	NP_001137283.1:p.Ala120Thr
NM_001143812.2:c.358G>A (BDNF)	NP_001137284.1:p.Ala120Thr
NM_001143816.2:c.358G>A (BDNF)	NP_001137288.1:p.Ala120Thr
NM_170733.4:c.358G>A (BDNF)	NP_733929.1:p.Ala120Thr
NM_170734.4:c.403G>A (BDNF)	NP_733930.1:p.Ala135Thr
NM_170735.6:c.358G>A (BDNF)	NP_733931.1:p.Ala120Thr