Canonical Allele Identifier: CA374315685
Gene: ABCA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.104806350C>T , CM000671.2:g.104806350C>T GRCh38
NC_000009.11:g.107568631C>T , CM000671.1:g.107568631C>T GRCh37
NC_000009.10:g.106608452C>T NCBI36
NG_007981.1:g.126806G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000374736.8:c.4355G>A MANE Select ENSP00000363868.3:p.Gly1452Glu
ENST00000678995.1:c.4361G>A ENSP00000504612.1:p.Gly1454Glu
ENST00000374736.7:c.4355G>A ENSP00000363868.3:p.Gly1452Glu
NM_005502.3:c.4355G>A NP_005493.2:p.Gly1452Glu
XM_005251773.1:c.4361G>A XP_005251830.1:p.Gly1454Glu
XM_005251776.1:c.4181G>A XP_005251833.1:p.Gly1394Glu
XM_011518339.1:c.4436G>A XP_011516641.1:p.Gly1479Glu
XM_011518340.1:c.4436G>A XP_011516642.1:p.Gly1479Glu
XM_011518341.1:c.4430G>A XP_011516643.1:p.Gly1477Glu
XM_011518342.1:c.3998G>A XP_011516644.1:p.Gly1333Glu
XM_011518343.1:c.4436G>A XP_011516645.1:p.Gly1479Glu
XM_011518344.1:c.4436G>A XP_011516646.1:p.Gly1479Glu
XM_005251773.3:c.4361G>A XP_005251830.1:p.Gly1454Glu
XM_005251776.3:c.4181G>A XP_005251833.1:p.Gly1394Glu
XM_011518339.3:c.4436G>A XP_011516641.1:p.Gly1479Glu
XM_011518340.3:c.4436G>A XP_011516642.1:p.Gly1479Glu
XM_011518341.3:c.4430G>A XP_011516643.1:p.Gly1477Glu
XM_011518342.3:c.3998G>A XP_011516644.1:p.Gly1333Glu
XM_011518344.2:c.4436G>A XP_011516646.1:p.Gly1479Glu
XM_017014378.2:c.4436G>A XP_016869867.1:p.Gly1479Glu
XM_017014379.2:c.4436G>A XP_016869868.1:p.Gly1479Glu
XM_017014380.2:c.4436G>A XP_016869869.1:p.Gly1479Glu
XM_017014381.2:c.4436G>A XP_016869870.1:p.Gly1479Glu
XM_017014382.2:c.4298G>A XP_016869871.1:p.Gly1433Glu
XR_001746223.1:n.4749G>A
NM_005502.4:c.4355G>A MANE Select NP_005493.2:p.Gly1452Glu