Canonical Allele Identifier: CA1918249826
Gene: NODAL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70435537A= , CM000672.2:g.70435537A= GRCh38
NC_000010.10:g.72195293A= , CM000672.1:g.72195293A= GRCh37
NC_000010.9:g.71865299A= NCBI36
NG_012448.1:g.11173T=
NG_012448.2:g.17412T=

Transcript Alleles

HGVS Amino-acid change
ENST00000287139.8:c.640T= MANE Select ENSP00000287139.3:p.Trp214=
ENST00000287139.7:c.640T= ENSP00000287139.3:p.Trp214=
ENST00000414871.1:c.475T= ENSP00000394468.1:p.Trp159=
NM_018055.4:c.640T= NP_060525.3:p.Trp214=
NM_001329906.1:c.241T= NP_001316835.1:p.Trp81=
XM_024448028.1:c.241T= XP_024303796.1:p.Trp81=
NM_018055.5:c.640T= MANE Select NP_060525.3:p.Trp214=
NM_001329906.2:c.241T= NP_001316835.1:p.Trp81=