Canonical Allele Identifier: CA376945702
Gene: NODAL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70435533T>A , CM000672.2:g.70435533T>A GRCh38
NC_000010.10:g.72195289T>A , CM000672.1:g.72195289T>A GRCh37
NC_000010.9:g.71865295T>A NCBI36
NG_012448.1:g.11177A>T
NG_012448.2:g.17416A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000287139.8:c.644A>T MANE Select ENSP00000287139.3:p.Glu215Val
ENST00000287139.7:c.644A>T ENSP00000287139.3:p.Glu215Val
ENST00000414871.1:c.479A>T ENSP00000394468.1:p.Glu160Val
NM_018055.4:c.644A>T NP_060525.3:p.Glu215Val
NM_001329906.1:c.245A>T NP_001316835.1:p.Glu82Val
XM_024448028.1:c.245A>T XP_024303796.1:p.Glu82Val
NM_018055.5:c.644A>T MANE Select NP_060525.3:p.Glu215Val
NM_001329906.2:c.245A>T NP_001316835.1:p.Glu82Val