Canonical Allele Identifier: CA1918249829
Gene: NODAL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70435544G= , CM000672.2:g.70435544G= GRCh38
NC_000010.10:g.72195300G= , CM000672.1:g.72195300G= GRCh37
NC_000010.9:g.71865306G= NCBI36
NG_012448.1:g.11166C=
NG_012448.2:g.17405C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000287139.8:c.633C= MANE Select ENSP00000287139.3:p.Thr211=
ENST00000287139.7:c.633C= ENSP00000287139.3:p.Thr211=
ENST00000414871.1:c.468C= ENSP00000394468.1:p.Thr156=
NM_018055.4:c.633C= NP_060525.3:p.Thr211=
NM_001329906.1:c.234C= NP_001316835.1:p.Thr78=
XM_024448028.1:c.234C= XP_024303796.1:p.Thr78=
NM_018055.5:c.633C= MANE Select NP_060525.3:p.Thr211=
NM_001329906.2:c.234C= NP_001316835.1:p.Thr78=