Canonical Allele Identifier: CA1869947623

Gene: ABCA1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.104884826_104884827delinsAG , CM000671.2:g.104884826_104884827delinsAG	GRCh38
NC_000009.11:g.107647107_107647108delinsAG , CM000671.1:g.107647107_107647108delinsAG	GRCh37
NC_000009.10:g.106686928_106686929delinsAG	NCBI36
NG_007981.1:g.48329_48330delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000374736.8:c.161-259_161-258delinsCT MANE Select	ENSP00000363868.3:n.161-259_161-258delinsCT
ENST00000678995.1:c.161-259_161-258delinsCT	ENSP00000504612.1:n.161-259_161-258delinsCT
ENST00000374733.1:c.-20-259_-20-258delinsCT	ENSP00000363865.1:n.-20-259_-20-258delinsCT
ENST00000374736.7:c.161-259_161-258delinsCT	ENSP00000363868.3:n.161-259_161-258delinsCT
ENST00000423487.6:c.161-259_161-258delinsCT	ENSP00000416623.2:n.161-259_161-258delinsCT
NM_005502.3:c.161-259_161-258delinsCT	NP_005493.2:n.161-259_161-258delinsCT
XM_005251773.1:c.161-259_161-258delinsCT	XP_005251830.1:n.161-259_161-258delinsCT
XM_005251776.1:c.-20-259_-20-258delinsCT	XP_005251833.1:n.-20-259_-20-258delinsCT
XM_011518339.1:c.236-259_236-258delinsCT	XP_011516641.1:n.236-259_236-258delinsCT
XM_011518340.1:c.236-259_236-258delinsCT	XP_011516642.1:n.236-259_236-258delinsCT
XM_011518341.1:c.236-259_236-258delinsCT	XP_011516643.1:n.236-259_236-258delinsCT
XM_011518342.1:c.-61-1670_-61-1669delinsCT	XP_011516644.1:n.-61-1670_-61-1669delinsCT
XM_011518343.1:c.236-259_236-258delinsCT	XP_011516645.1:n.236-259_236-258delinsCT
XM_011518344.1:c.236-259_236-258delinsCT	XP_011516646.1:n.236-259_236-258delinsCT
XM_005251773.3:c.161-259_161-258delinsCT	XP_005251830.1:n.161-259_161-258delinsCT
XM_005251776.3:c.-20-259_-20-258delinsCT	XP_005251833.1:n.-20-259_-20-258delinsCT
XM_011518339.3:c.236-259_236-258delinsCT	XP_011516641.1:n.236-259_236-258delinsCT
XM_011518340.3:c.236-259_236-258delinsCT	XP_011516642.1:n.236-259_236-258delinsCT
XM_011518341.3:c.236-259_236-258delinsCT	XP_011516643.1:n.236-259_236-258delinsCT
XM_011518342.3:c.-61-1670_-61-1669delinsCT	XP_011516644.1:n.-61-1670_-61-1669delinsCT
XM_011518344.2:c.236-259_236-258delinsCT	XP_011516646.1:n.236-259_236-258delinsCT
XM_017014378.2:c.236-259_236-258delinsCT	XP_016869867.1:n.236-259_236-258delinsCT
XM_017014379.2:c.236-259_236-258delinsCT	XP_016869868.1:n.236-259_236-258delinsCT
XM_017014380.2:c.236-259_236-258delinsCT	XP_016869869.1:n.236-259_236-258delinsCT
XM_017014381.2:c.236-259_236-258delinsCT	XP_016869870.1:n.236-259_236-258delinsCT
XM_017014382.2:c.98-259_98-258delinsCT	XP_016869871.1:n.98-259_98-258delinsCT
XR_001746223.1:n.549-259_549-258delinsCT
NM_005502.4:c.161-259_161-258delinsCT MANE Select	NP_005493.2:n.161-259_161-258delinsCT