Canonical Allele Identifier: CA376945728
Gene: NODAL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70435545G>C , CM000672.2:g.70435545G>C GRCh38
NC_000010.10:g.72195301G>C , CM000672.1:g.72195301G>C GRCh37
NC_000010.9:g.71865307G>C NCBI36
NG_012448.1:g.11165C>G
NG_012448.2:g.17404C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000287139.8:c.632C>G MANE Select ENSP00000287139.3:p.Thr211Ser
ENST00000287139.7:c.632C>G ENSP00000287139.3:p.Thr211Ser
ENST00000414871.1:c.467C>G ENSP00000394468.1:p.Thr156Ser
NM_018055.4:c.632C>G NP_060525.3:p.Thr211Ser
NM_001329906.1:c.233C>G NP_001316835.1:p.Thr78Ser
XM_024448028.1:c.233C>G XP_024303796.1:p.Thr78Ser
NM_018055.5:c.632C>G MANE Select NP_060525.3:p.Thr211Ser
NM_001329906.2:c.233C>G NP_001316835.1:p.Thr78Ser