Canonical Allele Identifier: CA376946064

Gene: NODAL

Linked Data

• MyVariant Identifiers: chr10:g.72195406A>G (hg19) ; chr10:g.70435650A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.70435650A>G , CM000672.2:g.70435650A>G	GRCh38
NC_000010.10:g.72195406A>G , CM000672.1:g.72195406A>G	GRCh37
NC_000010.9:g.71865412A>G	NCBI36
NG_012448.1:g.11060T>C
NG_012448.2:g.17299T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000287139.8:c.527T>C MANE Select	ENSP00000287139.3:p.Val176Ala
ENST00000287139.7:c.527T>C	ENSP00000287139.3:p.Val176Ala
ENST00000414871.1:c.362T>C	ENSP00000394468.1:p.Val121Ala
NM_018055.4:c.527T>C	NP_060525.3:p.Val176Ala
NM_001329906.1:c.128T>C	NP_001316835.1:p.Val43Ala
XM_024448028.1:c.128T>C	XP_024303796.1:p.Val43Ala
NM_018055.5:c.527T>C MANE Select	NP_060525.3:p.Val176Ala
NM_001329906.2:c.128T>C	NP_001316835.1:p.Val43Ala