Canonical Allele Identifier: CA376946038
Gene: NODAL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70435642C>A , CM000672.2:g.70435642C>A GRCh38
NC_000010.10:g.72195398C>A , CM000672.1:g.72195398C>A GRCh37
NC_000010.9:g.71865404C>A NCBI36
NG_012448.1:g.11068G>T
NG_012448.2:g.17307G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000287139.8:c.535G>T MANE Select ENSP00000287139.3:p.Glu179Ter
ENST00000287139.7:c.535G>T ENSP00000287139.3:p.Glu179Ter
ENST00000414871.1:c.370G>T ENSP00000394468.1:p.Glu124Ter
NM_018055.4:c.535G>T NP_060525.3:p.Glu179Ter
NM_001329906.1:c.136G>T NP_001316835.1:p.Glu46Ter
XM_024448028.1:c.136G>T XP_024303796.1:p.Glu46Ter
NM_018055.5:c.535G>T MANE Select NP_060525.3:p.Glu179Ter
NM_001329906.2:c.136G>T NP_001316835.1:p.Glu46Ter