Canonical Allele Identifier: CA1992591834

Gene: AMOTL1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.94800278G= , CM000673.2:g.94800278G=	GRCh38
NC_000011.9:g.94533444G= , CM000673.1:g.94533444G=	GRCh37
NC_000011.8:g.94173092G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_130847.3:c.1088G= MANE Select	NP_570899.1:p.Arg363=
ENST00000433060.3:c.1088G= MANE Select	ENSP00000387739.2:p.Arg363=
NM_001301007.1:c.938G=	NP_001287936.1:p.Arg313=
NM_001301007.2:c.938G=	NP_001287936.1:p.Arg313=
NM_130847.2:c.1088G=	NP_570899.1:p.Arg363=
ENST00000317829.12:c.938G=	ENSP00000320968.8:p.Arg313=
ENST00000433060.2:c.1088G=	ENSP00000387739.2:p.Arg363=
XM_005273798.3:c.1175G=	XP_005273855.1:p.Arg392=
XM_005273798.4:c.1175G=	XP_005273855.1:p.Arg392=
XM_005273801.3:c.830G=	XP_005273858.1:p.Arg277=
XM_005273801.4:c.830G=	XP_005273858.1:p.Arg277=
XM_006718772.2:c.1175G=	XP_006718835.1:p.Arg392=
XM_006718772.3:c.1175G=	XP_006718835.1:p.Arg392=
XM_011542626.1:c.1025G=	XP_011540928.1:p.Arg342=
XM_011542626.2:c.1025G=	XP_011540928.1:p.Arg342=
XM_011542627.1:c.830G=	XP_011540929.1:p.Arg277=