Canonical Allele Identifier: CA1869919568

Gene: ABCA1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.104828718_104828719delinsTG , CM000671.2:g.104828718_104828719delinsTG	GRCh38
NC_000009.11:g.107590999_107591000delinsTG , CM000671.1:g.107590999_107591000delinsTG	GRCh37
NC_000009.10:g.106630820_106630821delinsTG	NCBI36
NG_007981.1:g.104437_104438delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374736.8:c.2115+197_2115+198delinsCA MANE Select	ENSP00000363868.3:n.2115+197_2115+198delinsCA
ENST00000678995.1:c.2115+197_2115+198delinsCA	ENSP00000504612.1:n.2115+197_2115+198delinsCA
ENST00000374736.7:c.2115+197_2115+198delinsCA	ENSP00000363868.3:n.2115+197_2115+198delinsCA
ENST00000494467.1:n.288+197_288+198delinsCA
NM_005502.3:c.2115+197_2115+198delinsCA	NP_005493.2:n.2115+197_2115+198delinsCA
XM_005251773.1:c.2115+197_2115+198delinsCA	XP_005251830.1:n.2115+197_2115+198delinsCA
XM_005251776.1:c.1935+197_1935+198delinsCA	XP_005251833.1:n.1935+197_1935+198delinsCA
XM_011518339.1:c.2190+197_2190+198delinsCA	XP_011516641.1:n.2190+197_2190+198delinsCA
XM_011518340.1:c.2190+197_2190+198delinsCA	XP_011516642.1:n.2190+197_2190+198delinsCA
XM_011518341.1:c.2190+197_2190+198delinsCA	XP_011516643.1:n.2190+197_2190+198delinsCA
XM_011518342.1:c.1752+197_1752+198delinsCA	XP_011516644.1:n.1752+197_1752+198delinsCA
XM_011518343.1:c.2190+197_2190+198delinsCA	XP_011516645.1:n.2190+197_2190+198delinsCA
XM_011518344.1:c.2190+197_2190+198delinsCA	XP_011516646.1:n.2190+197_2190+198delinsCA
XM_005251773.3:c.2115+197_2115+198delinsCA	XP_005251830.1:n.2115+197_2115+198delinsCA
XM_005251776.3:c.1935+197_1935+198delinsCA	XP_005251833.1:n.1935+197_1935+198delinsCA
XM_011518339.3:c.2190+197_2190+198delinsCA	XP_011516641.1:n.2190+197_2190+198delinsCA
XM_011518340.3:c.2190+197_2190+198delinsCA	XP_011516642.1:n.2190+197_2190+198delinsCA
XM_011518341.3:c.2190+197_2190+198delinsCA	XP_011516643.1:n.2190+197_2190+198delinsCA
XM_011518342.3:c.1752+197_1752+198delinsCA	XP_011516644.1:n.1752+197_1752+198delinsCA
XM_011518344.2:c.2190+197_2190+198delinsCA	XP_011516646.1:n.2190+197_2190+198delinsCA
XM_017014378.2:c.2190+197_2190+198delinsCA	XP_016869867.1:n.2190+197_2190+198delinsCA
XM_017014379.2:c.2190+197_2190+198delinsCA	XP_016869868.1:n.2190+197_2190+198delinsCA
XM_017014380.2:c.2190+197_2190+198delinsCA	XP_016869869.1:n.2190+197_2190+198delinsCA
XM_017014381.2:c.2190+197_2190+198delinsCA	XP_016869870.1:n.2190+197_2190+198delinsCA
XM_017014382.2:c.2052+197_2052+198delinsCA	XP_016869871.1:n.2052+197_2052+198delinsCA
XR_001746223.1:n.2503+197_2503+198delinsCA
NM_005502.4:c.2115+197_2115+198delinsCA MANE Select	NP_005493.2:n.2115+197_2115+198delinsCA