Canonical Allele Identifier: CA504887489

Gene: ABCA7

Linked Data

• MyVariant Identifiers: chr19:g.1047224C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1047225C>T , CM000681.2:g.1047225C>T	GRCh38
NC_000019.9:g.1047224C>T , CM000681.1:g.1047224C>T	GRCh37
NC_000019.8:g.998224C>T	NCBI36
NG_046909.1:g.12123C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263094.11:c.1914C>T MANE Select	ENSP00000263094.6:p.Ala638=
ENST00000433129.6:n.2594C>T
ENST00000263094.10:c.1914C>T	ENSP00000263094.6:p.Ala638=
ENST00000433129.5:c.1914C>T	ENSP00000414062.1:p.Ala638=
ENST00000435683.6:c.1500C>T	ENSP00000465322.1:p.Ala500=
ENST00000533574.1:n.332C>T
NM_019112.3:c.1914C>T	NP_061985.2:p.Ala638=
XM_006722616.1:c.1914C>T	XP_006722679.1:p.Ala638=
XM_006722617.2:c.1914C>T	XP_006722680.1:p.Ala638=
XM_011527628.1:c.1914C>T	XP_011525930.1:p.Ala638=
XM_011527629.1:c.1914C>T	XP_011525931.1:p.Ala638=
XM_011527630.1:c.1914C>T	XP_011525932.1:p.Ala638=
XM_011527631.1:c.1914C>T	XP_011525933.1:p.Ala638=
XM_011527632.1:c.1458C>T	XP_011525934.1:p.Ala486=
XM_011527633.1:c.1914C>T	XP_011525935.1:p.Ala638=
XM_011527634.1:c.1914C>T	XP_011525936.1:p.Ala638=
XM_011527635.1:c.1914C>T	XP_011525937.1:p.Ala638=
XR_936148.1:n.2132C>T
XR_936149.1:n.2132C>T
XR_936150.1:n.2132C>T
XR_936151.1:n.2132C>T
XR_936152.1:n.2132C>T
XR_936153.1:n.2132C>T
XR_936154.1:n.2132C>T
XR_936155.1:n.2132C>T
XM_011527633.2:c.1914C>T	XP_011525935.1:p.Ala638=
XM_017026143.1:c.1914C>T	XP_016881632.1:p.Ala638=
XM_024451315.1:c.1914C>T	XP_024307083.1:p.Ala638=
XM_024451316.1:c.1914C>T	XP_024307084.1:p.Ala638=
XM_024451317.1:c.1914C>T	XP_024307085.1:p.Ala638=
XM_024451318.1:c.1914C>T	XP_024307086.1:p.Ala638=
XM_024451319.1:c.1914C>T	XP_024307087.1:p.Ala638=
XM_024451320.1:c.1914C>T	XP_024307088.1:p.Ala638=
XM_024451321.1:c.1914C>T	XP_024307089.1:p.Ala638=
XM_024451322.1:c.1458C>T	XP_024307090.1:p.Ala486=
XM_024451323.1:c.1914C>T	XP_024307091.1:p.Ala638=
XR_001753585.1:n.2132C>T
XR_001753586.1:n.2132C>T
XR_002958240.1:n.2132C>T
XR_002958241.1:n.2132C>T
XR_002958242.1:n.2132C>T
NM_019112.4:c.1914C>T MANE Select	NP_061985.2:p.Ala638=