Canonical Allele Identifier: CA376945714
Gene: NODAL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70435537A>C , CM000672.2:g.70435537A>C GRCh38
NC_000010.10:g.72195293A>C , CM000672.1:g.72195293A>C GRCh37
NC_000010.9:g.71865299A>C NCBI36
NG_012448.1:g.11173T>G
NG_012448.2:g.17412T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000287139.8:c.640T>G MANE Select ENSP00000287139.3:p.Trp214Gly
ENST00000287139.7:c.640T>G ENSP00000287139.3:p.Trp214Gly
ENST00000414871.1:c.475T>G ENSP00000394468.1:p.Trp159Gly
NM_018055.4:c.640T>G NP_060525.3:p.Trp214Gly
NM_001329906.1:c.241T>G NP_001316835.1:p.Trp81Gly
XM_024448028.1:c.241T>G XP_024303796.1:p.Trp81Gly
NM_018055.5:c.640T>G MANE Select NP_060525.3:p.Trp214Gly
NM_001329906.2:c.241T>G NP_001316835.1:p.Trp81Gly