Canonical Allele Identifier: CA376946061

Gene: NODAL

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000287139.8:c.529G>C MANE Select	ENSP00000287139.3:p.Ala177Pro
ENST00000287139.7:c.529G>C	ENSP00000287139.3:p.Ala177Pro
ENST00000414871.1:c.364G>C	ENSP00000394468.1:p.Ala122Pro
NM_018055.4:c.529G>C	NP_060525.3:p.Ala177Pro
NM_001329906.1:c.130G>C	NP_001316835.1:p.Ala44Pro
XM_024448028.1:c.130G>C	XP_024303796.1:p.Ala44Pro
NM_018055.5:c.529G>C MANE Select	NP_060525.3:p.Ala177Pro
NM_001329906.2:c.130G>C	NP_001316835.1:p.Ala44Pro