Canonical Allele Identifier: CA376945701
Gene: NODAL HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

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