Canonical Allele Identifier: CA1224646649

Gene: TMEM63A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.225852749C= , CM000663.2:g.225852749C=	GRCh38
NC_000001.10:g.226040450C= , CM000663.1:g.226040450C=	GRCh37
NC_000001.9:g.224107073C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366835.8:c.1818G= MANE Select	ENSP00000355800.3:p.Glu606=
ENST00000366835.7:c.1818G=	ENSP00000355800.3:p.Glu606=
NM_014698.2:c.1818G=	NP_055513.2:p.Glu606=
XM_006711841.2:c.1287G=	XP_006711904.1:p.Glu429=
XM_011544328.1:c.1818G=	XP_011542630.1:p.Glu606=
XM_011544329.1:c.1818G=	XP_011542631.1:p.Glu606=
XM_011544330.1:c.1818G=	XP_011542632.1:p.Glu606=
XM_011544331.1:c.1731G=	XP_011542633.1:p.Glu577=
XM_011544332.1:c.1377G=	XP_011542634.1:p.Glu459=
XR_949163.1:n.2123G=
XM_006711841.4:c.1287G=	XP_006711904.1:p.Glu429=
XM_011544328.3:c.1818G=	XP_011542630.1:p.Glu606=
XM_011544329.3:c.1818G=	XP_011542631.1:p.Glu606=
XM_011544330.3:c.1818G=	XP_011542632.1:p.Glu606=
XM_011544331.3:c.1731G=	XP_011542633.1:p.Glu577=
XM_011544332.3:c.1377G=	XP_011542634.1:p.Glu459=
XR_001737552.2:n.1905G=
XR_949163.3:n.2102G=
NM_014698.3:c.1818G= MANE Select	NP_055513.2:p.Glu606=