Canonical Allele Identifier: CA470278905
Gene: NODAL HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.72195402A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70435646A>T , CM000672.2:g.70435646A>T GRCh38
NC_000010.10:g.72195402A>T , CM000672.1:g.72195402A>T GRCh37
NC_000010.9:g.71865408A>T NCBI36
NG_012448.1:g.11064T>A
NG_012448.2:g.17303T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000287139.8:c.531T>A MANE Select ENSP00000287139.3:p.Ala177=
ENST00000287139.7:c.531T>A ENSP00000287139.3:p.Ala177=
ENST00000414871.1:c.366T>A ENSP00000394468.1:p.Ala122=
NM_018055.4:c.531T>A NP_060525.3:p.Ala177=
NM_001329906.1:c.132T>A NP_001316835.1:p.Ala44=
XM_024448028.1:c.132T>A XP_024303796.1:p.Ala44=
NM_018055.5:c.531T>A MANE Select NP_060525.3:p.Ala177=
NM_001329906.2:c.132T>A NP_001316835.1:p.Ala44=