Canonical Allele Identifier: CA376945742

Gene: NODAL

Linked Data

• MyVariant Identifiers: chr10:g.72195308C>A (hg19) ; chr10:g.70435552C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.70435552C>A , CM000672.2:g.70435552C>A	GRCh38
NC_000010.10:g.72195308C>A , CM000672.1:g.72195308C>A	GRCh37
NC_000010.9:g.71865314C>A	NCBI36
NG_012448.1:g.11158G>T
NG_012448.2:g.17397G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000287139.8:c.625G>T MANE Select	ENSP00000287139.3:p.Gly209Trp
ENST00000287139.7:c.625G>T	ENSP00000287139.3:p.Gly209Trp
ENST00000414871.1:c.460G>T	ENSP00000394468.1:p.Gly154Trp
NM_018055.4:c.625G>T	NP_060525.3:p.Gly209Trp
NM_001329906.1:c.226G>T	NP_001316835.1:p.Gly76Trp
XM_024448028.1:c.226G>T	XP_024303796.1:p.Gly76Trp
NM_018055.5:c.625G>T MANE Select	NP_060525.3:p.Gly209Trp
NM_001329906.2:c.226G>T	NP_001316835.1:p.Gly76Trp