Canonical Allele Identifier: CA5537558
Gene: NODAL HGNC NCBI

Linked Data

dbSNP Id: rs773777002

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000287139.8:c.640T>A MANE Select ENSP00000287139.3:p.Trp214Arg
ENST00000287139.7:c.640T>A ENSP00000287139.3:p.Trp214Arg
ENST00000414871.1:c.475T>A ENSP00000394468.1:p.Trp159Arg
NM_018055.4:c.640T>A NP_060525.3:p.Trp214Arg
NM_001329906.1:c.241T>A NP_001316835.1:p.Trp81Arg
XM_024448028.1:c.241T>A XP_024303796.1:p.Trp81Arg
NM_018055.5:c.640T>A MANE Select NP_060525.3:p.Trp214Arg
NM_001329906.2:c.241T>A NP_001316835.1:p.Trp81Arg