Canonical Allele Identifier: CA2317483012

Gene: ABCA7

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1047514_1047516delinsAGG , CM000681.2:g.1047514_1047516delinsAGG	GRCh38
NC_000019.9:g.1047513_1047515delinsAGG , CM000681.1:g.1047513_1047515delinsAGG	GRCh37
NC_000019.8:g.998513_998515delinsAGG	NCBI36
NG_046909.1:g.12412_12414delinsAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263094.11:c.2129_2131delinsAGG MANE Select	ENSP00000263094.6:p.Gln710=
ENST00000433129.6:n.2809_2811delinsAGG
ENST00000263094.10:c.2129_2131delinsAGG	ENSP00000263094.6:p.Gln710=
ENST00000433129.5:c.2129_2131delinsAGG	ENSP00000414062.1:p.Gln710=
ENST00000435683.6:c.1715_1717delinsAGG	ENSP00000465322.1:p.Gln572=
ENST00000533574.1:n.547_549delinsAGG
NM_019112.3:c.2129_2131delinsAGG	NP_061985.2:p.Gln710=
XM_006722616.1:c.2129_2131delinsAGG	XP_006722679.1:p.Gln710=
XM_006722617.2:c.2129_2131delinsAGG	XP_006722680.1:p.Gln710=
XM_011527628.1:c.2129_2131delinsAGG	XP_011525930.1:p.Gln710=
XM_011527629.1:c.2129_2131delinsAGG	XP_011525931.1:p.Gln710=
XM_011527630.1:c.2129_2131delinsAGG	XP_011525932.1:p.Gln710=
XM_011527631.1:c.2129_2131delinsAGG	XP_011525933.1:p.Gln710=
XM_011527632.1:c.1673_1675delinsAGG	XP_011525934.1:p.Gln558=
XM_011527633.1:c.2129_2131delinsAGG	XP_011525935.1:p.Gln710=
XM_011527634.1:c.2129_2131delinsAGG	XP_011525936.1:p.Gln710=
XM_011527635.1:c.2129_2131delinsAGG	XP_011525937.1:p.Gln710=
XR_936148.1:n.2347_2349delinsAGG
XR_936149.1:n.2347_2349delinsAGG
XR_936150.1:n.2347_2349delinsAGG
XR_936151.1:n.2347_2349delinsAGG
XR_936152.1:n.2347_2349delinsAGG
XR_936153.1:n.2347_2349delinsAGG
XR_936154.1:n.2347_2349delinsAGG
XR_936155.1:n.2347_2349delinsAGG
XM_011527633.2:c.2129_2131delinsAGG	XP_011525935.1:p.Gln710=
XM_017026143.1:c.2129_2131delinsAGG	XP_016881632.1:p.Gln710=
XM_024451315.1:c.2129_2131delinsAGG	XP_024307083.1:p.Gln710=
XM_024451316.1:c.2129_2131delinsAGG	XP_024307084.1:p.Gln710=
XM_024451317.1:c.2129_2131delinsAGG	XP_024307085.1:p.Gln710=
XM_024451318.1:c.2129_2131delinsAGG	XP_024307086.1:p.Gln710=
XM_024451319.1:c.2129_2131delinsAGG	XP_024307087.1:p.Gln710=
XM_024451320.1:c.2129_2131delinsAGG	XP_024307088.1:p.Gln710=
XM_024451321.1:c.2129_2131delinsAGG	XP_024307089.1:p.Gln710=
XM_024451322.1:c.1673_1675delinsAGG	XP_024307090.1:p.Gln558=
XM_024451323.1:c.2129_2131delinsAGG	XP_024307091.1:p.Gln710=
XR_001753585.1:n.2347_2349delinsAGG
XR_001753586.1:n.2347_2349delinsAGG
XR_002958240.1:n.2347_2349delinsAGG
XR_002958241.1:n.2347_2349delinsAGG
XR_002958242.1:n.2347_2349delinsAGG
NM_019112.4:c.2129_2131delinsAGG MANE Select	NP_061985.2:p.Gln710=