Canonical Allele Identifier: CA1539963227

Gene: GDNF

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37815827T= , CM000667.2:g.37815827T=	GRCh38
NC_000005.9:g.37815929T= , CM000667.1:g.37815929T=	GRCh37
NC_000005.8:g.37851686T=	NCBI36
NG_011675.2:g.28854A=

Transcript Alleles

HGVS	Amino-acid Change
NM_000514.4:c.460A= MANE Select	NP_000505.1:p.Thr154=
ENST00000326524.7:c.460A= MANE Select	ENSP00000317145.2:p.Thr154=
NM_000514.3:c.460A=	NP_000505.1:p.Thr154=
NM_001190468.1:c.511A=	NP_001177397.1:p.Thr171=
NM_001190469.1:c.433A=	NP_001177398.1:p.Thr145=
NM_001278098.1:c.304A=	NP_001265027.1:p.Thr102=
NM_199231.2:c.382A=	NP_954701.1:p.Thr128=
ENST00000326524.6:c.460A=	ENSP00000317145.2:p.Thr154=
ENST00000344622.8:c.382A=	ENSP00000339703.4:p.Thr128=
ENST00000381826.8:c.433A=	ENSP00000371248.4:p.Thr145=
ENST00000427982.5:c.511A=	ENSP00000409007.1:p.Thr171=
ENST00000515058.5:c.382A=	ENSP00000425928.1:p.Thr128=
ENST00000620847.1:c.304A=	ENSP00000478722.1:p.Thr102=
XM_011514028.1:c.460A=	XP_011512330.1:p.Thr154=
XM_011514029.1:c.460A=	XP_011512331.1:p.Thr154=
XM_011514030.1:c.304A=	XP_011512332.1:p.Thr102=
XM_011514030.3:c.304A=	XP_011512332.1:p.Thr102=
XM_017009337.2:c.382A=	XP_016864826.1:p.Thr128=