Canonical Allele Identifier: CA1869953658

Gene: ABCA1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.104822329_104822330delinsCA , CM000671.2:g.104822329_104822330delinsCA	GRCh38
NC_000009.11:g.107584610_107584611delinsCA , CM000671.1:g.107584610_107584611delinsCA	GRCh37
NC_000009.10:g.106624431_106624432delinsCA	NCBI36
NG_007981.1:g.110826_110827delinsTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000374736.8:c.2828+166_2828+167delinsTG MANE Select	ENSP00000363868.3:n.2828+166_2828+167deli...
ENST00000678995.1:c.2828+166_2828+167delinsTG	ENSP00000504612.1:n.2828+166_2828+167deli...
ENST00000374736.7:c.2828+166_2828+167delinsTG	ENSP00000363868.3:n.2828+166_2828+167deli...
NM_005502.3:c.2828+166_2828+167delinsTG	NP_005493.2:n.2828+166_2828+167delinsTG
XM_005251773.1:c.2828+166_2828+167delinsTG	XP_005251830.1:n.2828+166_2828+167delinsT...
XM_005251776.1:c.2648+166_2648+167delinsTG	XP_005251833.1:n.2648+166_2648+167delinsT...
XM_011518339.1:c.2903+166_2903+167delinsTG	XP_011516641.1:n.2903+166_2903+167delinsT...
XM_011518340.1:c.2903+166_2903+167delinsTG	XP_011516642.1:n.2903+166_2903+167delinsT...
XM_011518341.1:c.2903+166_2903+167delinsTG	XP_011516643.1:n.2903+166_2903+167delinsT...
XM_011518342.1:c.2465+166_2465+167delinsTG	XP_011516644.1:n.2465+166_2465+167delinsT...
XM_011518343.1:c.2903+166_2903+167delinsTG	XP_011516645.1:n.2903+166_2903+167delinsT...
XM_011518344.1:c.2903+166_2903+167delinsTG	XP_011516646.1:n.2903+166_2903+167delinsT...
XM_005251773.3:c.2828+166_2828+167delinsTG	XP_005251830.1:n.2828+166_2828+167delinsT...
XM_005251776.3:c.2648+166_2648+167delinsTG	XP_005251833.1:n.2648+166_2648+167delinsT...
XM_011518339.3:c.2903+166_2903+167delinsTG	XP_011516641.1:n.2903+166_2903+167delinsT...
XM_011518340.3:c.2903+166_2903+167delinsTG	XP_011516642.1:n.2903+166_2903+167delinsT...
XM_011518341.3:c.2903+166_2903+167delinsTG	XP_011516643.1:n.2903+166_2903+167delinsT...
XM_011518342.3:c.2465+166_2465+167delinsTG	XP_011516644.1:n.2465+166_2465+167delinsT...
XM_011518344.2:c.2903+166_2903+167delinsTG	XP_011516646.1:n.2903+166_2903+167delinsT...
XM_017014378.2:c.2903+166_2903+167delinsTG	XP_016869867.1:n.2903+166_2903+167delinsT...
XM_017014379.2:c.2903+166_2903+167delinsTG	XP_016869868.1:n.2903+166_2903+167delinsT...
XM_017014380.2:c.2903+166_2903+167delinsTG	XP_016869869.1:n.2903+166_2903+167delinsT...
XM_017014381.2:c.2903+166_2903+167delinsTG	XP_016869870.1:n.2903+166_2903+167delinsT...
XM_017014382.2:c.2765+166_2765+167delinsTG	XP_016869871.1:n.2765+166_2765+167delinsT...
XR_001746223.1:n.3216+166_3216+167delinsTG
NM_005502.4:c.2828+166_2828+167delinsTG MANE Select	NP_005493.2:n.2828+166_2828+167delinsTG