Canonical Allele Identifier: CA402976318

Gene: ABCA7

Linked Data

• dbSNP Id: rs113809142
• MyVariant Identifiers: chr19:g.1056244T>A (hg19) ; chr19:g.1056245T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1056245T>A , CM000681.2:g.1056245T>A	GRCh38
NC_000019.9:g.1056244T>A , CM000681.1:g.1056244T>A	GRCh37
NC_000019.8:g.1007244T>A	NCBI36
NG_046909.1:g.21143T>A

Transcript Alleles

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