Canonical Allele Identifier: CA9033311
Gene: ABCA7 HGNC NCBI

Linked Data

ClinVar Variation Id: 225544
dbSNP Id: rs547447016

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1047511_1047517del , CM000681.2:g.1047511_1047517del GRCh38
NC_000019.9:g.1047510_1047516del , CM000681.1:g.1047510_1047516del GRCh37
NC_000019.8:g.998510_998516del NCBI36
NG_046909.1:g.12409_12415del

Transcript Alleles

HGVS Amino-acid change
ENST00000263094.11:c.2126_2132del MANE Select ENSP00000263094.6:p.Glu709AlafsTer?
ENST00000433129.6:n.2806_2812del
ENST00000263094.10:c.2126_2132del ENSP00000263094.6:p.Glu709AlafsTer?
ENST00000433129.5:c.2126_2132del ENSP00000414062.1:p.Glu709AlafsTer?
ENST00000435683.6:c.1712_1718del ENSP00000465322.1:p.Glu571AlafsTer?
ENST00000533574.1:n.544_550del
NM_019112.3:c.2126_2132del NP_061985.2:p.Glu709AlafsTer?
XM_006722616.1:c.2126_2132del XP_006722679.1:p.Glu709AlafsTer?
XM_006722617.2:c.2126_2132del XP_006722680.1:p.Glu709AlafsTer?
XM_011527628.1:c.2126_2132del XP_011525930.1:p.Glu709AlafsTer?
XM_011527629.1:c.2126_2132del XP_011525931.1:p.Glu709AlafsTer?
XM_011527630.1:c.2126_2132del XP_011525932.1:p.Glu709AlafsTer?
XM_011527631.1:c.2126_2132del XP_011525933.1:p.Glu709AlafsTer?
XM_011527632.1:c.1670_1676del XP_011525934.1:p.Glu557AlafsTer?
XM_011527633.1:c.2126_2132del XP_011525935.1:p.Glu709AlafsTer?
XM_011527634.1:c.2126_2132del XP_011525936.1:p.Glu709AlafsTer?
XM_011527635.1:c.2126_2132del XP_011525937.1:p.Glu709AlafsTer?
XR_936148.1:n.2344_2350del
XR_936149.1:n.2344_2350del
XR_936150.1:n.2344_2350del
XR_936151.1:n.2344_2350del
XR_936152.1:n.2344_2350del
XR_936153.1:n.2344_2350del
XR_936154.1:n.2344_2350del
XR_936155.1:n.2344_2350del
XM_011527633.2:c.2126_2132del XP_011525935.1:p.Glu709AlafsTer?
XM_017026143.1:c.2126_2132del XP_016881632.1:p.Glu709AlafsTer?
XM_024451315.1:c.2126_2132del XP_024307083.1:p.Glu709AlafsTer?
XM_024451316.1:c.2126_2132del XP_024307084.1:p.Glu709AlafsTer?
XM_024451317.1:c.2126_2132del XP_024307085.1:p.Glu709AlafsTer?
XM_024451318.1:c.2126_2132del XP_024307086.1:p.Glu709AlafsTer?
XM_024451319.1:c.2126_2132del XP_024307087.1:p.Glu709AlafsTer?
XM_024451320.1:c.2126_2132del XP_024307088.1:p.Glu709AlafsTer?
XM_024451321.1:c.2126_2132del XP_024307089.1:p.Glu709AlafsTer?
XM_024451322.1:c.1670_1676del XP_024307090.1:p.Glu557AlafsTer?
XM_024451323.1:c.2126_2132del XP_024307091.1:p.Glu709AlafsTer?
XR_001753585.1:n.2344_2350del
XR_001753586.1:n.2344_2350del
XR_002958240.1:n.2344_2350del
XR_002958241.1:n.2344_2350del
XR_002958242.1:n.2344_2350del
NM_019112.4:c.2126_2132del MANE Select NP_061985.2:p.Glu709AlafsTer?