Canonical Allele Identifier: CA2317479104

Gene: ABCA7

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1041068_1041069delinsCT , CM000681.2:g.1041068_1041069delinsCT	GRCh38
NC_000019.9:g.1041067_1041068delinsCT , CM000681.1:g.1041067_1041068delinsCT	GRCh37
NC_000019.8:g.992067_992068delinsCT	NCBI36
NG_046909.1:g.5966_5967delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263094.11:c.-137-157_-137-156delinsCT MANE Select	ENSP00000263094.6:n.-137-157_-137-156delinsCT
ENST00000433129.6:n.201-157_201-156delinsCT
ENST00000263094.10:c.-137-157_-137-156delinsCT	ENSP00000263094.6:n.-137-157_-137-156delinsCT
ENST00000524850.5:c.-7-287_-7-286delinsCT	ENSP00000431473.1:n.-7-287_-7-286delinsCT
ENST00000525238.2:n.80-157_80-156delinsCT
ENST00000526885.5:n.95-157_95-156delinsCT
ENST00000530703.1:n.82-157_82-156delinsCT
ENST00000611490.4:c.-137-157_-137-156delinsCT	ENSP00000478857.1:n.-137-157_-137-156delinsCT
NM_019112.3:c.-137-157_-137-156delinsCT	NP_061985.2:n.-137-157_-137-156delinsCT
XM_006722616.1:c.-137-157_-137-156delinsCT	XP_006722679.1:n.-137-157_-137-156delinsCT
XM_006722617.2:c.-137-157_-137-156delinsCT	XP_006722680.1:n.-137-157_-137-156delinsCT
XM_011527628.1:c.-7-287_-7-286delinsCT	XP_011525930.1:n.-7-287_-7-286delinsCT
XM_011527629.1:c.-137-157_-137-156delinsCT	XP_011525931.1:n.-137-157_-137-156delinsCT
XM_011527630.1:c.-137-157_-137-156delinsCT	XP_011525932.1:n.-137-157_-137-156delinsCT
XM_011527631.1:c.-137-157_-137-156delinsCT	XP_011525933.1:n.-137-157_-137-156delinsCT
XM_011527633.1:c.-137-157_-137-156delinsCT	XP_011525935.1:n.-137-157_-137-156delinsCT
XM_011527634.1:c.-137-157_-137-156delinsCT	XP_011525936.1:n.-137-157_-137-156delinsCT
XM_011527635.1:c.-137-157_-137-156delinsCT	XP_011525937.1:n.-137-157_-137-156delinsCT
XR_936148.1:n.82-157_82-156delinsCT
XR_936149.1:n.82-157_82-156delinsCT
XR_936150.1:n.82-157_82-156delinsCT
XR_936151.1:n.82-157_82-156delinsCT
XR_936152.1:n.82-157_82-156delinsCT
XR_936153.1:n.82-157_82-156delinsCT
XR_936154.1:n.82-157_82-156delinsCT
XR_936155.1:n.82-157_82-156delinsCT
XM_011527633.2:c.-137-157_-137-156delinsCT	XP_011525935.1:n.-137-157_-137-156delinsCT
XM_017026143.1:c.-137-157_-137-156delinsCT	XP_016881632.1:n.-137-157_-137-156delinsCT
XM_024451315.1:c.-137-157_-137-156delinsCT	XP_024307083.1:n.-137-157_-137-156delinsCT
XM_024451316.1:c.-7-287_-7-286delinsCT	XP_024307084.1:n.-7-287_-7-286delinsCT
XM_024451317.1:c.-137-157_-137-156delinsCT	XP_024307085.1:n.-137-157_-137-156delinsCT
XM_024451318.1:c.-137-157_-137-156delinsCT	XP_024307086.1:n.-137-157_-137-156delinsCT
XM_024451319.1:c.-137-157_-137-156delinsCT	XP_024307087.1:n.-137-157_-137-156delinsCT
XM_024451320.1:c.-137-157_-137-156delinsCT	XP_024307088.1:n.-137-157_-137-156delinsCT
XM_024451321.1:c.-137-157_-137-156delinsCT	XP_024307089.1:n.-137-157_-137-156delinsCT
XM_024451323.1:c.-137-157_-137-156delinsCT	XP_024307091.1:n.-137-157_-137-156delinsCT
XR_001753585.1:n.82-157_82-156delinsCT
XR_001753586.1:n.82-157_82-156delinsCT
XR_002958240.1:n.82-157_82-156delinsCT
XR_002958241.1:n.82-157_82-156delinsCT
XR_002958242.1:n.82-157_82-156delinsCT
NM_019112.4:c.-137-157_-137-156delinsCT MANE Select	NP_061985.2:n.-137-157_-137-156delinsCT