Canonical Allele Identifier: CA1539963244

Gene: GDNF

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37815839C= , CM000667.2:g.37815839C=	GRCh38
NC_000005.9:g.37815941C= , CM000667.1:g.37815941C=	GRCh37
NC_000005.8:g.37851698C=	NCBI36
NG_011675.2:g.28842G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326524.7:c.448G= MANE Select	ENSP00000317145.2:p.Asp150=
ENST00000326524.6:c.448G=	ENSP00000317145.2:p.Asp150=
ENST00000344622.8:c.370G=	ENSP00000339703.4:p.Asp124=
ENST00000381826.8:c.421G=	ENSP00000371248.4:p.Asp141=
ENST00000427982.5:c.499G=	ENSP00000409007.1:p.Asp167=
ENST00000515058.5:c.370G=	ENSP00000425928.1:p.Asp124=
ENST00000620847.1:c.292G=	ENSP00000478722.1:p.Asp98=
NM_000514.3:c.448G=	NP_000505.1:p.Asp150=
NM_001190468.1:c.499G=	NP_001177397.1:p.Asp167=
NM_001190469.1:c.421G=	NP_001177398.1:p.Asp141=
NM_001278098.1:c.292G=	NP_001265027.1:p.Asp98=
NM_199231.2:c.370G=	NP_954701.1:p.Asp124=
XM_011514028.1:c.448G=	XP_011512330.1:p.Asp150=
XM_011514029.1:c.448G=	XP_011512331.1:p.Asp150=
XM_011514030.1:c.292G=	XP_011512332.1:p.Asp98=
XM_011514030.3:c.292G=	XP_011512332.1:p.Asp98=
XM_017009337.2:c.370G=	XP_016864826.1:p.Asp124=
NM_000514.4:c.448G= MANE Select	NP_000505.1:p.Asp150=