Canonical Allele Identifier: CA376946062

Gene: NODAL

Linked Data

• MyVariant Identifiers: chr10:g.72195404C>T (hg19) ; chr10:g.70435648C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.70435648C>T , CM000672.2:g.70435648C>T	GRCh38
NC_000010.10:g.72195404C>T , CM000672.1:g.72195404C>T	GRCh37
NC_000010.9:g.71865410C>T	NCBI36
NG_012448.1:g.11062G>A
NG_012448.2:g.17301G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000287139.8:c.529G>A MANE Select	ENSP00000287139.3:p.Ala177Thr
ENST00000287139.7:c.529G>A	ENSP00000287139.3:p.Ala177Thr
ENST00000414871.1:c.364G>A	ENSP00000394468.1:p.Ala122Thr
NM_018055.4:c.529G>A	NP_060525.3:p.Ala177Thr
NM_001329906.1:c.130G>A	NP_001316835.1:p.Ala44Thr
XM_024448028.1:c.130G>A	XP_024303796.1:p.Ala44Thr
NM_018055.5:c.529G>A MANE Select	NP_060525.3:p.Ala177Thr
NM_001329906.2:c.130G>A	NP_001316835.1:p.Ala44Thr