Canonical Allele Identifier: CA2588185742

Gene: ABCA7

Linked Data

• gnomAD v4: 19-1047738-TGGGGGTG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1047747_1047753del , CM000681.2:g.1047747_1047753del	GRCh38
NC_000019.9:g.1047746_1047752del , CM000681.1:g.1047746_1047752del	GRCh37
NC_000019.8:g.998746_998752del	NCBI36
NG_046909.1:g.12645_12651del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263094.11:c.2269+93_2269+99del MANE Select	ENSP00000263094.6:n.2269+93_2269+99del
ENST00000433129.6:n.2949+93_2949+99del
ENST00000263094.10:c.2269+93_2269+99del	ENSP00000263094.6:n.2269+93_2269+99del
ENST00000433129.5:c.2269+93_2269+99del	ENSP00000414062.1:n.2269+93_2269+99del
ENST00000435683.6:c.1855+93_1855+99del	ENSP00000465322.1:n.1855+93_1855+99del
NM_019112.3:c.2269+93_2269+99del	NP_061985.2:n.2269+93_2269+99del
XM_006722616.1:c.2269+93_2269+99del	XP_006722679.1:n.2269+93_2269+99del
XM_006722617.2:c.2269+93_2269+99del	XP_006722680.1:n.2269+93_2269+99del
XM_006722618.2:c.-23+93_-23+99del	XP_006722681.1:n.-23+93_-23+99del
XM_011527628.1:c.2269+93_2269+99del	XP_011525930.1:n.2269+93_2269+99del
XM_011527629.1:c.2269+93_2269+99del	XP_011525931.1:n.2269+93_2269+99del
XM_011527630.1:c.2269+93_2269+99del	XP_011525932.1:n.2269+93_2269+99del
XM_011527631.1:c.2269+93_2269+99del	XP_011525933.1:n.2269+93_2269+99del
XM_011527632.1:c.1813+93_1813+99del	XP_011525934.1:n.1813+93_1813+99del
XM_011527633.1:c.2269+93_2269+99del	XP_011525935.1:n.2269+93_2269+99del
XM_011527634.1:c.2269+93_2269+99del	XP_011525936.1:n.2269+93_2269+99del
XM_011527635.1:c.2269+93_2269+99del	XP_011525937.1:n.2269+93_2269+99del
XM_011527636.1:c.-23+116_-23+122del	XP_011525938.1:n.-23+116_-23+122del
XR_936148.1:n.2487+93_2487+99del
XR_936149.1:n.2487+93_2487+99del
XR_936150.1:n.2487+93_2487+99del
XR_936151.1:n.2487+93_2487+99del
XR_936152.1:n.2487+93_2487+99del
XR_936153.1:n.2487+93_2487+99del
XR_936154.1:n.2487+93_2487+99del
XR_936155.1:n.2487+93_2487+99del
XM_011527633.2:c.2269+93_2269+99del	XP_011525935.1:n.2269+93_2269+99del
XM_017026143.1:c.2269+93_2269+99del	XP_016881632.1:n.2269+93_2269+99del
XM_024451315.1:c.2269+93_2269+99del	XP_024307083.1:n.2269+93_2269+99del
XM_024451316.1:c.2269+93_2269+99del	XP_024307084.1:n.2269+93_2269+99del
XM_024451317.1:c.2269+93_2269+99del	XP_024307085.1:n.2269+93_2269+99del
XM_024451318.1:c.2269+93_2269+99del	XP_024307086.1:n.2269+93_2269+99del
XM_024451319.1:c.2269+93_2269+99del	XP_024307087.1:n.2269+93_2269+99del
XM_024451320.1:c.2269+93_2269+99del	XP_024307088.1:n.2269+93_2269+99del
XM_024451321.1:c.2269+93_2269+99del	XP_024307089.1:n.2269+93_2269+99del
XM_024451322.1:c.1813+93_1813+99del	XP_024307090.1:n.1813+93_1813+99del
XM_024451323.1:c.2269+93_2269+99del	XP_024307091.1:n.2269+93_2269+99del
XM_024451324.1:c.-23+93_-23+99del	XP_024307092.1:n.-23+93_-23+99del
XM_024451325.1:c.-23+116_-23+122del	XP_024307093.1:n.-23+116_-23+122del
XR_001753585.1:n.2487+93_2487+99del
XR_001753586.1:n.2487+93_2487+99del
XR_002958240.1:n.2487+93_2487+99del
XR_002958241.1:n.2487+93_2487+99del
XR_002958242.1:n.2487+93_2487+99del
NM_019112.4:c.2269+93_2269+99del MANE Select	NP_061985.2:n.2269+93_2269+99del