Canonical Allele Identifier: CA1630848649

Gene: BDNF

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.27700731G= , CM000673.2:g.27700731G=	GRCh38
NC_000011.9:g.27722278G= , CM000673.1:g.27722278G=	GRCh37
NC_000011.8:g.27678854G=	NCBI36
NG_011794.1:g.26328C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001143805.1:c.-22+19913C=	NP_001137277.1:n.-22+19913C=
NM_001143806.1:c.-22+19698C=	NP_001137278.1:n.-22+19698C=
NM_001143807.1:c.-22+18780C=	NP_001137279.1:n.-22+18780C=
NM_001143807.2:c.-22+18780C=	NP_001137279.1:n.-22+18780C=
NM_001143808.1:c.-22+250C=	NP_001137280.1:n.-22+250C=
NM_001143808.2:c.-22+250C=	NP_001137280.1:n.-22+250C=
NM_001143809.1:c.66+240C=	NP_001137281.1:n.66+240C=
NM_001143809.2:c.66+240C=	NP_001137281.1:n.66+240C=
NM_001143810.1:c.-59+240C=	NP_001137282.1:n.-59+240C=
NM_001143810.2:c.-59+240C=	NP_001137282.1:n.-59+240C=
NM_001143811.1:c.-422+240C=	NP_001137283.1:n.-422+240C=
NM_001143811.2:c.-422+240C=	NP_001137283.1:n.-422+240C=
NM_001143812.1:c.-77C=	NP_001137284.1:n.-77C=
NM_001143812.2:c.-77C=	NP_001137284.1:n.-77C=
NM_170731.4:c.3+20681C=	NP_733927.1:n.3+20681C=
NM_170731.5:c.3+20681C=	NP_733927.1:n.3+20681C=
NM_170732.4:c.-22+19615C=	NP_733928.1:n.-22+19615C=
NM_170733.3:c.-22+566C=	NP_733929.1:n.-22+566C=
NM_170733.4:c.-22+566C=	NP_733929.1:n.-22+566C=
ENST00000314915.6:c.3+20681C=	ENSP00000320002.6:n.3+20681C=
ENST00000395978.7:c.-22+19698C=	ENSP00000379302.3:n.-22+19698C=
ENST00000395980.6:c.-22+566C=	ENSP00000379304.2:n.-22+566C=
ENST00000395981.7:c.-22+19615C=	ENSP00000379305.3:n.-22+19615C=
ENST00000395983.7:c.-22+240C=	ENSP00000379307.3:n.-22+240C=
ENST00000420794.2:c.-422+240C=	ENSP00000389564.1:n.-422+240C=
ENST00000438929.5:c.-59+240C=	ENSP00000414303.1:n.-59+240C=
ENST00000525950.5:c.-22+19913C=	ENSP00000432035.1:n.-22+19913C=
ENST00000530786.5:c.-59+240C=	ENSP00000433003.1:n.-59+240C=
ENST00000530861.5:c.-77C=	ENSP00000435564.1:n.-77C=
ENST00000532997.5:c.-22+18780C=	ENSP00000435805.1:n.-22+18780C=
ENST00000584049.5:n.337+566C=