Canonical Allele Identifier: CA1869915068
Gene: ABCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.104825780C= , CM000671.2:g.104825780C= GRCh38
NC_000009.11:g.107588061C= , CM000671.1:g.107588061C= GRCh37
NC_000009.10:g.106627882C= NCBI36
NG_007981.1:g.107376G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374736.8:c.2445G= MANE Select ENSP00000363868.3:p.Glu815=
ENST00000678995.1:c.2445G= ENSP00000504612.1:p.Glu815=
ENST00000374736.7:c.2445G= ENSP00000363868.3:p.Glu815=
ENST00000494467.1:n.618G=
NM_005502.3:c.2445G= NP_005493.2:p.Glu815=
XM_005251773.1:c.2445G= XP_005251830.1:p.Glu815=
XM_005251776.1:c.2265G= XP_005251833.1:p.Glu755=
XM_011518339.1:c.2520G= XP_011516641.1:p.Glu840=
XM_011518340.1:c.2520G= XP_011516642.1:p.Glu840=
XM_011518341.1:c.2520G= XP_011516643.1:p.Glu840=
XM_011518342.1:c.2082G= XP_011516644.1:p.Glu694=
XM_011518343.1:c.2520G= XP_011516645.1:p.Glu840=
XM_011518344.1:c.2520G= XP_011516646.1:p.Glu840=
XM_005251773.3:c.2445G= XP_005251830.1:p.Glu815=
XM_005251776.3:c.2265G= XP_005251833.1:p.Glu755=
XM_011518339.3:c.2520G= XP_011516641.1:p.Glu840=
XM_011518340.3:c.2520G= XP_011516642.1:p.Glu840=
XM_011518341.3:c.2520G= XP_011516643.1:p.Glu840=
XM_011518342.3:c.2082G= XP_011516644.1:p.Glu694=
XM_011518344.2:c.2520G= XP_011516646.1:p.Glu840=
XM_017014378.2:c.2520G= XP_016869867.1:p.Glu840=
XM_017014379.2:c.2520G= XP_016869868.1:p.Glu840=
XM_017014380.2:c.2520G= XP_016869869.1:p.Glu840=
XM_017014381.2:c.2520G= XP_016869870.1:p.Glu840=
XM_017014382.2:c.2382G= XP_016869871.1:p.Glu794=
XR_001746223.1:n.2833G=
NM_005502.4:c.2445G= MANE Select NP_005493.2:p.Glu815=