Canonical Allele Identifier: CA1455390256

Gene: ATP10D

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.47561431G= , CM000666.2:g.47561431G=	GRCh38
NC_000004.11:g.47563448G= , CM000666.1:g.47563448G=	GRCh37
NC_000004.10:g.47258205G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273859.8:c.2668+356G= MANE Select	ENSP00000273859.3:n.2668+356G=
ENST00000273859.7:c.2668+356G=	ENSP00000273859.3:n.2668+356G=
ENST00000503288.6:c.1023+356G=
NM_020453.3:c.2668+356G=	NP_065186.3:n.2668+356G=
XM_005248119.3:c.2623+356G=	XP_005248176.1:n.2623+356G=
XM_005248120.3:c.2668+356G=	XP_005248177.1:n.2668+356G=
XM_011513722.1:c.2473+356G=	XP_011512024.1:n.2473+356G=
XM_011513723.1:c.1192+356G=	XP_011512025.1:n.1192+356G=
XR_925154.1:n.2954+356G=
XM_005248119.4:c.2623+356G=	XP_005248176.1:n.2623+356G=
XM_005248120.4:c.2668+356G=	XP_005248177.1:n.2668+356G=
XM_011513722.2:c.2473+356G=	XP_011512024.1:n.2473+356G=
XM_017008472.1:c.1192+356G=	XP_016863961.1:n.1192+356G=
XR_001741295.1:n.2919+356G=
XR_925154.2:n.2950+356G=
NM_020453.4:c.2668+356G= MANE Select	NP_065186.3:n.2668+356G=