Canonical Allele Identifier: CA359613683

Gene: GDNF

Linked Data

• MyVariant Identifiers: chr5:g.37815769C>G (hg19) ; chr5:g.37815667C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37815667C>G , CM000667.2:g.37815667C>G	GRCh38
NC_000005.9:g.37815769C>G , CM000667.1:g.37815769C>G	GRCh37
NC_000005.8:g.37851526C>G	NCBI36
NG_011675.2:g.29014G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000326524.7:c.620G>C MANE Select	ENSP00000317145.2:p.Arg207Thr
ENST00000326524.6:c.620G>C	ENSP00000317145.2:p.Arg207Thr
ENST00000344622.8:c.542G>C	ENSP00000339703.4:p.Arg181Thr
ENST00000381826.8:c.593G>C	ENSP00000371248.4:p.Arg198Thr
ENST00000427982.5:c.671G>C	ENSP00000409007.1:p.Arg224Thr
ENST00000515058.5:c.542G>C	ENSP00000425928.1:p.Arg181Thr
ENST00000620847.1:c.464G>C	ENSP00000478722.1:p.Arg155Thr
NM_000514.3:c.620G>C	NP_000505.1:p.Arg207Thr
NM_001190468.1:c.671G>C	NP_001177397.1:p.Arg224Thr
NM_001190469.1:c.593G>C	NP_001177398.1:p.Arg198Thr
NM_001278098.1:c.464G>C	NP_001265027.1:p.Arg155Thr
NM_199231.2:c.542G>C	NP_954701.1:p.Arg181Thr
XM_011514028.1:c.620G>C	XP_011512330.1:p.Arg207Thr
XM_011514029.1:c.620G>C	XP_011512331.1:p.Arg207Thr
XM_011514030.1:c.464G>C	XP_011512332.1:p.Arg155Thr
XM_011514030.3:c.464G>C	XP_011512332.1:p.Arg155Thr
XM_017009337.2:c.542G>C	XP_016864826.1:p.Arg181Thr
NM_000514.4:c.620G>C MANE Select	NP_000505.1:p.Arg207Thr