Canonical Allele Identifier: CA2317489454
Gene: ABCA7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1056265G= , CM000681.2:g.1056265G= GRCh38
NC_000019.9:g.1056264G= , CM000681.1:g.1056264G= GRCh37
NC_000019.8:g.1007264G= NCBI36
NG_046909.1:g.21163G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263094.11:c.4416+22G= MANE Select ENSP00000263094.6:n.4416+22G=
ENST00000433129.6:n.4716+22G=
ENST00000435683.7:c.1901+22G= ENSP00000465322.2:n.1901+22G=
ENST00000673773.1:n.259+22G=
ENST00000263094.10:c.4416+22G= ENSP00000263094.6:n.4416+22G=
ENST00000433129.5:c.4416+22G= ENSP00000414062.1:n.4416+22G=
ENST00000435683.6:c.4002+22G= ENSP00000465322.1:n.4002+22G=
NM_019112.3:c.4416+22G= NP_061985.2:n.4416+22G=
XM_006722616.1:c.4416+22G= XP_006722679.1:n.4416+22G=
XM_006722617.2:c.4416+22G= XP_006722680.1:n.4416+22G=
XM_006722618.2:c.2073+22G= XP_006722681.1:n.2073+22G=
XM_011527628.1:c.4416+22G= XP_011525930.1:n.4416+22G=
XM_011527629.1:c.4389+22G= XP_011525931.1:n.4389+22G=
XM_011527630.1:c.4416+22G= XP_011525932.1:n.4416+22G=
XM_011527631.1:c.4416+22G= XP_011525933.1:n.4416+22G=
XM_011527632.1:c.3960+22G= XP_011525934.1:n.3960+22G=
XM_011527633.1:c.4416+22G= XP_011525935.1:n.4416+22G=
XM_011527634.1:c.4416+22G= XP_011525936.1:n.4416+22G=
XM_011527635.1:c.4416+22G= XP_011525937.1:n.4416+22G=
XM_011527636.1:c.2073+22G= XP_011525938.1:n.2073+22G=
XR_936148.1:n.4634+22G=
XR_936149.1:n.4634+22G=
XR_936150.1:n.4634+22G=
XR_936151.1:n.4634+22G=
XR_936152.1:n.4634+22G=
XR_936153.1:n.4634+22G=
XR_936154.1:n.4634+22G=
XM_011527633.2:c.4416+22G= XP_011525935.1:n.4416+22G=
XM_017026143.1:c.4416+22G= XP_016881632.1:n.4416+22G=
XM_024451315.1:c.4416+22G= XP_024307083.1:n.4416+22G=
XM_024451316.1:c.4416+22G= XP_024307084.1:n.4416+22G=
XM_024451317.1:c.4389+22G= XP_024307085.1:n.4389+22G=
XM_024451318.1:c.4416+22G= XP_024307086.1:n.4416+22G=
XM_024451319.1:c.4416+22G= XP_024307087.1:n.4416+22G=
XM_024451320.1:c.4161+22G= XP_024307088.1:n.4161+22G=
XM_024451321.1:c.4416+22G= XP_024307089.1:n.4416+22G=
XM_024451322.1:c.3960+22G= XP_024307090.1:n.3960+22G=
XM_024451323.1:c.4416+22G= XP_024307091.1:n.4416+22G=
XM_024451324.1:c.2073+22G= XP_024307092.1:n.2073+22G=
XM_024451325.1:c.2073+22G= XP_024307093.1:n.2073+22G=
XR_001753585.1:n.4634+22G=
XR_001753586.1:n.4634+22G=
XR_002958240.1:n.4634+22G=
XR_002958241.1:n.4634+22G=
XR_002958242.1:n.4634+22G=
NM_019112.4:c.4416+22G= MANE Select NP_061985.2:n.4416+22G=