Canonical Allele Identifier: CA1918249831

Gene: NODAL

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.70435549A= , CM000672.2:g.70435549A=	GRCh38
NC_000010.10:g.72195305A= , CM000672.1:g.72195305A=	GRCh37
NC_000010.9:g.71865311A=	NCBI36
NG_012448.1:g.11161T=
NG_012448.2:g.17400T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000287139.8:c.628T= MANE Select	ENSP00000287139.3:p.Ser210=
ENST00000287139.7:c.628T=	ENSP00000287139.3:p.Ser210=
ENST00000414871.1:c.463T=	ENSP00000394468.1:p.Ser155=
NM_018055.4:c.628T=	NP_060525.3:p.Ser210=
NM_001329906.1:c.229T=	NP_001316835.1:p.Ser77=
XM_024448028.1:c.229T=	XP_024303796.1:p.Ser77=
NM_018055.5:c.628T= MANE Select	NP_060525.3:p.Ser210=
NM_001329906.2:c.229T=	NP_001316835.1:p.Ser77=