Canonical Allele Identifier: CA376945725
Gene: NODAL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70435543A>C , CM000672.2:g.70435543A>C GRCh38
NC_000010.10:g.72195299A>C , CM000672.1:g.72195299A>C GRCh37
NC_000010.9:g.71865305A>C NCBI36
NG_012448.1:g.11167T>G
NG_012448.2:g.17406T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000287139.8:c.634T>G MANE Select ENSP00000287139.3:p.Leu212Val
ENST00000287139.7:c.634T>G ENSP00000287139.3:p.Leu212Val
ENST00000414871.1:c.469T>G ENSP00000394468.1:p.Leu157Val
NM_018055.4:c.634T>G NP_060525.3:p.Leu212Val
NM_001329906.1:c.235T>G NP_001316835.1:p.Leu79Val
XM_024448028.1:c.235T>G XP_024303796.1:p.Leu79Val
NM_018055.5:c.634T>G MANE Select NP_060525.3:p.Leu212Val
NM_001329906.2:c.235T>G NP_001316835.1:p.Leu79Val