Canonical Allele Identifier: CA1539962542

Gene: GDNF

Linked Data

• dbSNP Id: rs1749885571
• gnomAD v4: 5-37815556-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37815556C>T , CM000667.2:g.37815556C>T	GRCh38
NC_000005.9:g.37815658C>T , CM000667.1:g.37815658C>T	GRCh37
NC_000005.8:g.37851415C>T	NCBI36
NG_011675.2:g.29125G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000326524.7:c.*95G>A MANE Select	ENSP00000317145.2:n.*95G>A
ENST00000326524.6:c.*95G>A	ENSP00000317145.2:n.*95G>A
ENST00000344622.8:c.*95G>A	ENSP00000339703.4:n.*95G>A
ENST00000620847.1:c.*95G>A	ENSP00000478722.1:n.*95G>A
NM_000514.3:c.*95G>A	NP_000505.1:n.*95G>A
NM_001190468.1:c.*95G>A	NP_001177397.1:n.*95G>A
NM_001190469.1:c.*95G>A	NP_001177398.1:n.*95G>A
NM_001278098.1:c.*95G>A	NP_001265027.1:n.*95G>A
NM_199231.2:c.*95G>A	NP_954701.1:n.*95G>A
XM_011514028.1:c.*95G>A	XP_011512330.1:n.*95G>A
XM_011514029.1:c.*95G>A	XP_011512331.1:n.*95G>A
XM_011514030.1:c.*95G>A	XP_011512332.1:n.*95G>A
XM_011514030.3:c.*95G>A	XP_011512332.1:n.*95G>A
XM_017009337.2:c.*95G>A	XP_016864826.1:n.*95G>A
NM_000514.4:c.*95G>A MANE Select	NP_000505.1:n.*95G>A