Canonical Allele Identifier: CA376946002
Gene: NODAL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70435634C>T , CM000672.2:g.70435634C>T GRCh38
NC_000010.10:g.72195390C>T , CM000672.1:g.72195390C>T GRCh37
NC_000010.9:g.71865396C>T NCBI36
NG_012448.1:g.11076G>A
NG_012448.2:g.17315G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000287139.8:c.543G>A MANE Select ENSP00000287139.3:p.Trp181Ter
ENST00000287139.7:c.543G>A ENSP00000287139.3:p.Trp181Ter
ENST00000414871.1:c.378G>A ENSP00000394468.1:p.Trp126Ter
NM_018055.4:c.543G>A NP_060525.3:p.Trp181Ter
NM_001329906.1:c.144G>A NP_001316835.1:p.Trp48Ter
XM_024448028.1:c.144G>A XP_024303796.1:p.Trp48Ter
NM_018055.5:c.543G>A MANE Select NP_060525.3:p.Trp181Ter
NM_001329906.2:c.144G>A NP_001316835.1:p.Trp48Ter