Canonical Allele Identifier: CA1539959940

Gene: GDNF

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37814375T= , CM000667.2:g.37814375T=	GRCh38
NC_000005.9:g.37814477T= , CM000667.1:g.37814477T=	GRCh37
NC_000005.8:g.37850234T=	NCBI36
NG_011675.2:g.30306A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326524.7:c.*1276A= MANE Select	ENSP00000317145.2:n.*1276A=
ENST00000326524.6:c.*1276A=	ENSP00000317145.2:n.*1276A=
ENST00000344622.8:c.*1276A=	ENSP00000339703.4:n.*1276A=
ENST00000620847.1:c.*1276A=	ENSP00000478722.1:n.*1276A=
NM_000514.3:c.*1276A=	NP_000505.1:n.*1276A=
NM_001190468.1:c.*1276A=	NP_001177397.1:n.*1276A=
NM_001190469.1:c.*1276A=	NP_001177398.1:n.*1276A=
NM_001278098.1:c.*1276A=	NP_001265027.1:n.*1276A=
NM_199231.2:c.*1276A=	NP_954701.1:n.*1276A=
XM_011514028.1:c.*1276A=	XP_011512330.1:n.*1276A=
XM_011514029.1:c.*1276A=	XP_011512331.1:n.*1276A=
XM_011514030.1:c.*1276A=	XP_011512332.1:n.*1276A=
NM_000514.4:c.*1276A= MANE Select	NP_000505.1:n.*1276A=