Canonical Allele Identifier: CA376946079

Gene: NODAL

Linked Data

• MyVariant Identifiers: chr10:g.72195409C>A (hg19) ; chr10:g.70435653C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.70435653C>A , CM000672.2:g.70435653C>A	GRCh38
NC_000010.10:g.72195409C>A , CM000672.1:g.72195409C>A	GRCh37
NC_000010.9:g.71865415C>A	NCBI36
NG_012448.1:g.11057G>T
NG_012448.2:g.17296G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000287139.8:c.524G>T MANE Select	ENSP00000287139.3:p.Arg175Met
ENST00000287139.7:c.524G>T	ENSP00000287139.3:p.Arg175Met
ENST00000414871.1:c.359G>T	ENSP00000394468.1:p.Arg120Met
NM_018055.4:c.524G>T	NP_060525.3:p.Arg175Met
NM_001329906.1:c.125G>T	NP_001316835.1:p.Arg42Met
XM_024448028.1:c.125G>T	XP_024303796.1:p.Arg42Met
NM_018055.5:c.524G>T MANE Select	NP_060525.3:p.Arg175Met
NM_001329906.2:c.125G>T	NP_001316835.1:p.Arg42Met