Canonical Allele Identifier: CA376945731
Gene: NODAL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70435546T>C , CM000672.2:g.70435546T>C GRCh38
NC_000010.10:g.72195302T>C , CM000672.1:g.72195302T>C GRCh37
NC_000010.9:g.71865308T>C NCBI36
NG_012448.1:g.11164A>G
NG_012448.2:g.17403A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000287139.8:c.631A>G MANE Select ENSP00000287139.3:p.Thr211Ala
ENST00000287139.7:c.631A>G ENSP00000287139.3:p.Thr211Ala
ENST00000414871.1:c.466A>G ENSP00000394468.1:p.Thr156Ala
NM_018055.4:c.631A>G NP_060525.3:p.Thr211Ala
NM_001329906.1:c.232A>G NP_001316835.1:p.Thr78Ala
XM_024448028.1:c.232A>G XP_024303796.1:p.Thr78Ala
NM_018055.5:c.631A>G MANE Select NP_060525.3:p.Thr211Ala
NM_001329906.2:c.232A>G NP_001316835.1:p.Thr78Ala