Canonical Allele Identifier: CA359613661

Gene: GDNF

Linked Data

• MyVariant Identifiers: chr5:g.37815760C>G (hg19) ; chr5:g.37815658C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37815658C>G , CM000667.2:g.37815658C>G	GRCh38
NC_000005.9:g.37815760C>G , CM000667.1:g.37815760C>G	GRCh37
NC_000005.8:g.37851517C>G	NCBI36
NG_011675.2:g.29023G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000326524.7:c.629G>C MANE Select	ENSP00000317145.2:p.Cys210Ser
ENST00000326524.6:c.629G>C	ENSP00000317145.2:p.Cys210Ser
ENST00000344622.8:c.551G>C	ENSP00000339703.4:p.Cys184Ser
ENST00000381826.8:c.602G>C	ENSP00000371248.4:p.Cys201Ser
ENST00000427982.5:c.680G>C	ENSP00000409007.1:p.Cys227Ser
ENST00000515058.5:c.551G>C	ENSP00000425928.1:p.Cys184Ser
ENST00000620847.1:c.473G>C	ENSP00000478722.1:p.Cys158Ser
NM_000514.3:c.629G>C	NP_000505.1:p.Cys210Ser
NM_001190468.1:c.680G>C	NP_001177397.1:p.Cys227Ser
NM_001190469.1:c.602G>C	NP_001177398.1:p.Cys201Ser
NM_001278098.1:c.473G>C	NP_001265027.1:p.Cys158Ser
NM_199231.2:c.551G>C	NP_954701.1:p.Cys184Ser
XM_011514028.1:c.629G>C	XP_011512330.1:p.Cys210Ser
XM_011514029.1:c.629G>C	XP_011512331.1:p.Cys210Ser
XM_011514030.1:c.473G>C	XP_011512332.1:p.Cys158Ser
XM_011514030.3:c.473G>C	XP_011512332.1:p.Cys158Ser
XM_017009337.2:c.551G>C	XP_016864826.1:p.Cys184Ser
NM_000514.4:c.629G>C MANE Select	NP_000505.1:p.Cys210Ser