Canonical Allele Identifier: CA2588188564

Gene: ABCA7

Linked Data

• gnomAD v4: 19-1055969-G-GCC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1055972_1055973dup , CM000681.2:g.1055972_1055973dup	GRCh38
NC_000019.9:g.1055971_1055972dup , CM000681.1:g.1055971_1055972dup	GRCh37
NC_000019.8:g.1006971_1006972dup	NCBI36
NG_046909.1:g.20870_20871dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263094.11:c.4238+33_4238+34dup MANE Select	ENSP00000263094.6:n.4238+33_4238+34dup
ENST00000433129.6:n.4538+33_4538+34dup
ENST00000435683.7:c.1723+33_1723+34dup	ENSP00000465322.2:n.1723+33_1723+34dup
ENST00000263094.10:c.4238+33_4238+34dup	ENSP00000263094.6:n.4238+33_4238+34dup
ENST00000433129.5:c.4238+33_4238+34dup	ENSP00000414062.1:n.4238+33_4238+34dup
ENST00000435683.6:c.3824+33_3824+34dup	ENSP00000465322.1:n.3824+33_3824+34dup
NM_019112.3:c.4238+33_4238+34dup	NP_061985.2:n.4238+33_4238+34dup
XM_006722616.1:c.4238+33_4238+34dup	XP_006722679.1:n.4238+33_4238+34dup
XM_006722617.2:c.4238+33_4238+34dup	XP_006722680.1:n.4238+33_4238+34dup
XM_006722618.2:c.1895+33_1895+34dup	XP_006722681.1:n.1895+33_1895+34dup
XM_011527628.1:c.4238+33_4238+34dup	XP_011525930.1:n.4238+33_4238+34dup
XM_011527629.1:c.4211+33_4211+34dup	XP_011525931.1:n.4211+33_4211+34dup
XM_011527630.1:c.4238+33_4238+34dup	XP_011525932.1:n.4238+33_4238+34dup
XM_011527631.1:c.4238+33_4238+34dup	XP_011525933.1:n.4238+33_4238+34dup
XM_011527632.1:c.3782+33_3782+34dup	XP_011525934.1:n.3782+33_3782+34dup
XM_011527633.1:c.4238+33_4238+34dup	XP_011525935.1:n.4238+33_4238+34dup
XM_011527634.1:c.4238+33_4238+34dup	XP_011525936.1:n.4238+33_4238+34dup
XM_011527635.1:c.4238+33_4238+34dup	XP_011525937.1:n.4238+33_4238+34dup
XM_011527636.1:c.1895+33_1895+34dup	XP_011525938.1:n.1895+33_1895+34dup
XR_936148.1:n.4456+33_4456+34dup
XR_936149.1:n.4456+33_4456+34dup
XR_936150.1:n.4456+33_4456+34dup
XR_936151.1:n.4456+33_4456+34dup
XR_936152.1:n.4456+33_4456+34dup
XR_936153.1:n.4456+33_4456+34dup
XR_936154.1:n.4456+33_4456+34dup
XM_011527633.2:c.4238+33_4238+34dup	XP_011525935.1:n.4238+33_4238+34dup
XM_017026143.1:c.4238+33_4238+34dup	XP_016881632.1:n.4238+33_4238+34dup
XM_024451315.1:c.4238+33_4238+34dup	XP_024307083.1:n.4238+33_4238+34dup
XM_024451316.1:c.4238+33_4238+34dup	XP_024307084.1:n.4238+33_4238+34dup
XM_024451317.1:c.4211+33_4211+34dup	XP_024307085.1:n.4211+33_4211+34dup
XM_024451318.1:c.4238+33_4238+34dup	XP_024307086.1:n.4238+33_4238+34dup
XM_024451319.1:c.4238+33_4238+34dup	XP_024307087.1:n.4238+33_4238+34dup
XM_024451320.1:c.3983+33_3983+34dup	XP_024307088.1:n.3983+33_3983+34dup
XM_024451321.1:c.4238+33_4238+34dup	XP_024307089.1:n.4238+33_4238+34dup
XM_024451322.1:c.3782+33_3782+34dup	XP_024307090.1:n.3782+33_3782+34dup
XM_024451323.1:c.4238+33_4238+34dup	XP_024307091.1:n.4238+33_4238+34dup
XM_024451324.1:c.1895+33_1895+34dup	XP_024307092.1:n.1895+33_1895+34dup
XM_024451325.1:c.1895+33_1895+34dup	XP_024307093.1:n.1895+33_1895+34dup
XR_001753585.1:n.4456+33_4456+34dup
XR_001753586.1:n.4456+33_4456+34dup
XR_002958240.1:n.4456+33_4456+34dup
XR_002958241.1:n.4456+33_4456+34dup
XR_002958242.1:n.4456+33_4456+34dup
NM_019112.4:c.4238+33_4238+34dup MANE Select	NP_061985.2:n.4238+33_4238+34dup