Canonical Allele Identifier: CA1539962758

Gene: GDNF

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37815663A= , CM000667.2:g.37815663A=	GRCh38
NC_000005.9:g.37815765A= , CM000667.1:g.37815765A=	GRCh37
NC_000005.8:g.37851522A=	NCBI36
NG_011675.2:g.29018T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000326524.7:c.624T= MANE Select	ENSP00000317145.2:p.Cys208=
ENST00000326524.6:c.624T=	ENSP00000317145.2:p.Cys208=
ENST00000344622.8:c.546T=	ENSP00000339703.4:p.Cys182=
ENST00000381826.8:c.597T=	ENSP00000371248.4:p.Cys199=
ENST00000427982.5:c.675T=	ENSP00000409007.1:p.Cys225=
ENST00000515058.5:c.546T=	ENSP00000425928.1:p.Cys182=
ENST00000620847.1:c.468T=	ENSP00000478722.1:p.Cys156=
NM_000514.3:c.624T=	NP_000505.1:p.Cys208=
NM_001190468.1:c.675T=	NP_001177397.1:p.Cys225=
NM_001190469.1:c.597T=	NP_001177398.1:p.Cys199=
NM_001278098.1:c.468T=	NP_001265027.1:p.Cys156=
NM_199231.2:c.546T=	NP_954701.1:p.Cys182=
XM_011514028.1:c.624T=	XP_011512330.1:p.Cys208=
XM_011514029.1:c.624T=	XP_011512331.1:p.Cys208=
XM_011514030.1:c.468T=	XP_011512332.1:p.Cys156=
XM_011514030.3:c.468T=	XP_011512332.1:p.Cys156=
XM_017009337.2:c.546T=	XP_016864826.1:p.Cys182=
NM_000514.4:c.624T= MANE Select	NP_000505.1:p.Cys208=