Canonical Allele Identifier: CA1918249872
Gene: NODAL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70435641T= , CM000672.2:g.70435641T= GRCh38
NC_000010.10:g.72195397T= , CM000672.1:g.72195397T= GRCh37
NC_000010.9:g.71865403T= NCBI36
NG_012448.1:g.11069A=
NG_012448.2:g.17308A=

Transcript Alleles

HGVS Amino-acid change
ENST00000287139.8:c.536A= MANE Select ENSP00000287139.3:p.Glu179=
ENST00000287139.7:c.536A= ENSP00000287139.3:p.Glu179=
ENST00000414871.1:c.371A= ENSP00000394468.1:p.Glu124=
NM_018055.4:c.536A= NP_060525.3:p.Glu179=
NM_001329906.1:c.137A= NP_001316835.1:p.Glu46=
XM_024448028.1:c.137A= XP_024303796.1:p.Glu46=
NM_018055.5:c.536A= MANE Select NP_060525.3:p.Glu179=
NM_001329906.2:c.137A= NP_001316835.1:p.Glu46=