Canonical Allele Identifier: CA1869959308
Gene: ABCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.104915065C= , CM000671.2:g.104915065C= GRCh38
NC_000009.11:g.107677346C= , CM000671.1:g.107677346C= GRCh37
NC_000009.10:g.106717167C= NCBI36
NG_007981.1:g.18091G=

Transcript Alleles

HGVS Amino-acid change
ENST00000374736.8:c.-92-11294G= MANE Select ENSP00000363868.3:n.-92-11294G=
ENST00000678995.1:c.-92-11294G= ENSP00000504612.1:n.-92-11294G=
ENST00000374733.1:c.-115+12870G= ENSP00000363865.1:n.-115+12870G=
ENST00000374736.7:c.-92-11294G= ENSP00000363868.3:n.-92-11294G=
ENST00000423487.6:c.-92-11294G= ENSP00000416623.2:n.-92-11294G=
NM_005502.3:c.-92-11294G= NP_005493.2:n.-92-11294G=
XM_005251773.1:c.-92-11294G= XP_005251830.1:n.-92-11294G=
XM_005251776.1:c.-115+12870G= XP_005251833.1:n.-115+12870G=
XM_011518339.1:c.-92-11294G= XP_011516641.1:n.-92-11294G=
XM_011518341.1:c.-92-11294G= XP_011516643.1:n.-92-11294G=
XM_011518342.1:c.-156+12870G= XP_011516644.1:n.-156+12870G=
XM_011518343.1:c.-92-11294G= XP_011516645.1:n.-92-11294G=
XM_011518344.1:c.-92-11294G= XP_011516646.1:n.-92-11294G=
XR_428585.2:n.999-3597C=
XR_428586.2:n.999-3597C=
XR_428587.2:n.20+2725C=
XM_005251773.3:c.-92-11294G= XP_005251830.1:n.-92-11294G=
XM_005251776.3:c.-115+12870G= XP_005251833.1:n.-115+12870G=
XM_011518339.3:c.-92-11294G= XP_011516641.1:n.-92-11294G=
XM_011518341.3:c.-92-11294G= XP_011516643.1:n.-92-11294G=
XM_011518342.3:c.-156+12870G= XP_011516644.1:n.-156+12870G=
XM_011518344.2:c.-92-11294G= XP_011516646.1:n.-92-11294G=
XR_001746223.1:n.222-11294G=
NM_005502.4:c.-92-11294G= MANE Select NP_005493.2:n.-92-11294G=