Canonical Allele Identifier: CA376945700
Gene: NODAL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70435532T>A , CM000672.2:g.70435532T>A GRCh38
NC_000010.10:g.72195288T>A , CM000672.1:g.72195288T>A GRCh37
NC_000010.9:g.71865294T>A NCBI36
NG_012448.1:g.11178A>T
NG_012448.2:g.17417A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000287139.8:c.645A>T MANE Select ENSP00000287139.3:p.Glu215Asp
ENST00000287139.7:c.645A>T ENSP00000287139.3:p.Glu215Asp
ENST00000414871.1:c.480A>T ENSP00000394468.1:p.Glu160Asp
NM_018055.4:c.645A>T NP_060525.3:p.Glu215Asp
NM_001329906.1:c.246A>T NP_001316835.1:p.Glu82Asp
XM_024448028.1:c.246A>T XP_024303796.1:p.Glu82Asp
NM_018055.5:c.645A>T MANE Select NP_060525.3:p.Glu215Asp
NM_001329906.2:c.246A>T NP_001316835.1:p.Glu82Asp