Canonical Allele Identifier: CA1918249789

Gene: NODAL

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.70435446C= , CM000672.2:g.70435446C=	GRCh38
NC_000010.10:g.72195202C= , CM000672.1:g.72195202C=	GRCh37
NC_000010.9:g.71865208C=	NCBI36
NG_012448.1:g.11264G=
NG_012448.2:g.17503G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000287139.8:c.731G= MANE Select	ENSP00000287139.3:p.Ser244=
ENST00000287139.7:c.731G=	ENSP00000287139.3:p.Ser244=
ENST00000414871.1:c.566G=	ENSP00000394468.1:p.Ser189=
NM_018055.4:c.731G=	NP_060525.3:p.Ser244=
NM_001329906.1:c.332G=	NP_001316835.1:p.Ser111=
XM_024448028.1:c.332G=	XP_024303796.1:p.Ser111=
NM_018055.5:c.731G= MANE Select	NP_060525.3:p.Ser244=
NM_001329906.2:c.332G=	NP_001316835.1:p.Ser111=