Canonical Allele Identifier: CA1918249832
Gene: NODAL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70435550C= , CM000672.2:g.70435550C= GRCh38
NC_000010.10:g.72195306C= , CM000672.1:g.72195306C= GRCh37
NC_000010.9:g.71865312C= NCBI36
NG_012448.1:g.11160G=
NG_012448.2:g.17399G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000287139.8:c.627G= MANE Select ENSP00000287139.3:p.Gly209=
ENST00000287139.7:c.627G= ENSP00000287139.3:p.Gly209=
ENST00000414871.1:c.462G= ENSP00000394468.1:p.Gly154=
NM_018055.4:c.627G= NP_060525.3:p.Gly209=
NM_001329906.1:c.228G= NP_001316835.1:p.Gly76=
XM_024448028.1:c.228G= XP_024303796.1:p.Gly76=
NM_018055.5:c.627G= MANE Select NP_060525.3:p.Gly209=
NM_001329906.2:c.228G= NP_001316835.1:p.Gly76=