Canonical Allele Identifier: CA376946057

Gene: NODAL

Linked Data

• MyVariant Identifiers: chr10:g.72195403G>T (hg19) ; chr10:g.70435647G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.70435647G>T , CM000672.2:g.70435647G>T	GRCh38
NC_000010.10:g.72195403G>T , CM000672.1:g.72195403G>T	GRCh37
NC_000010.9:g.71865409G>T	NCBI36
NG_012448.1:g.11063C>A
NG_012448.2:g.17302C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000287139.8:c.530C>A MANE Select	ENSP00000287139.3:p.Ala177Asp
ENST00000287139.7:c.530C>A	ENSP00000287139.3:p.Ala177Asp
ENST00000414871.1:c.365C>A	ENSP00000394468.1:p.Ala122Asp
NM_018055.4:c.530C>A	NP_060525.3:p.Ala177Asp
NM_001329906.1:c.131C>A	NP_001316835.1:p.Ala44Asp
XM_024448028.1:c.131C>A	XP_024303796.1:p.Ala44Asp
NM_018055.5:c.530C>A MANE Select	NP_060525.3:p.Ala177Asp
NM_001329906.2:c.131C>A	NP_001316835.1:p.Ala44Asp