Canonical Allele Identifier: CA376946003
Gene: NODAL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70435635C>A , CM000672.2:g.70435635C>A GRCh38
NC_000010.10:g.72195391C>A , CM000672.1:g.72195391C>A GRCh37
NC_000010.9:g.71865397C>A NCBI36
NG_012448.1:g.11075G>T
NG_012448.2:g.17314G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000287139.8:c.542G>T MANE Select ENSP00000287139.3:p.Trp181Leu
ENST00000287139.7:c.542G>T ENSP00000287139.3:p.Trp181Leu
ENST00000414871.1:c.377G>T ENSP00000394468.1:p.Trp126Leu
NM_018055.4:c.542G>T NP_060525.3:p.Trp181Leu
NM_001329906.1:c.143G>T NP_001316835.1:p.Trp48Leu
XM_024448028.1:c.143G>T XP_024303796.1:p.Trp48Leu
NM_018055.5:c.542G>T MANE Select NP_060525.3:p.Trp181Leu
NM_001329906.2:c.143G>T NP_001316835.1:p.Trp48Leu