Canonical Allele Identifier: CA1539963698

Gene: GDNF

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37816010G= , CM000667.2:g.37816010G=	GRCh38
NC_000005.9:g.37816112G= , CM000667.1:g.37816112G=	GRCh37
NC_000005.8:g.37851869G=	NCBI36
NG_011675.2:g.28671C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000514.4:c.277C= MANE Select	NP_000505.1:p.Arg93=
ENST00000326524.7:c.277C= MANE Select	ENSP00000317145.2:p.Arg93=
NM_000514.3:c.277C=	NP_000505.1:p.Arg93=
NM_001190468.1:c.328C=	NP_001177397.1:p.Arg110=
NM_001190469.1:c.250C=	NP_001177398.1:p.Arg84=
NM_001278098.1:c.121C=	NP_001265027.1:p.Arg41=
NM_199231.2:c.199C=	NP_954701.1:p.Arg67=
ENST00000326524.6:c.277C=	ENSP00000317145.2:p.Arg93=
ENST00000344622.8:c.199C=	ENSP00000339703.4:p.Arg67=
ENST00000381826.8:c.250C=	ENSP00000371248.4:p.Arg84=
ENST00000427982.5:c.328C=	ENSP00000409007.1:p.Arg110=
ENST00000515058.5:c.199C=	ENSP00000425928.1:p.Arg67=
ENST00000620847.1:c.121C=	ENSP00000478722.1:p.Arg41=
XM_011514028.1:c.277C=	XP_011512330.1:p.Arg93=
XM_011514029.1:c.277C=	XP_011512331.1:p.Arg93=
XM_011514030.1:c.121C=	XP_011512332.1:p.Arg41=
XM_011514030.3:c.121C=	XP_011512332.1:p.Arg41=
XM_017009337.2:c.199C=	XP_016864826.1:p.Arg67=