Canonical Allele Identifier: CA5168468
Gene: ABCA1 HGNC NCBI

Linked Data

dbSNP Id: rs746693787

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.104818818T>C , CM000671.2:g.104818818T>C GRCh38
NC_000009.11:g.107581099T>C , CM000671.1:g.107581099T>C GRCh37
NC_000009.10:g.106620920T>C NCBI36
NG_007981.1:g.114338A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000374736.8:c.3307A>G MANE Select ENSP00000363868.3:p.Ile1103Val
ENST00000678995.1:c.3307A>G ENSP00000504612.1:p.Ile1103Val
ENST00000374736.7:c.3307A>G ENSP00000363868.3:p.Ile1103Val
NM_005502.3:c.3307A>G NP_005493.2:p.Ile1103Val
XM_005251773.1:c.3307A>G XP_005251830.1:p.Ile1103Val
XM_005251776.1:c.3127A>G XP_005251833.1:p.Ile1043Val
XM_011518339.1:c.3382A>G XP_011516641.1:p.Ile1128Val
XM_011518340.1:c.3382A>G XP_011516642.1:p.Ile1128Val
XM_011518341.1:c.3382A>G XP_011516643.1:p.Ile1128Val
XM_011518342.1:c.2944A>G XP_011516644.1:p.Ile982Val
XM_011518343.1:c.3382A>G XP_011516645.1:p.Ile1128Val
XM_011518344.1:c.3382A>G XP_011516646.1:p.Ile1128Val
XM_005251773.3:c.3307A>G XP_005251830.1:p.Ile1103Val
XM_005251776.3:c.3127A>G XP_005251833.1:p.Ile1043Val
XM_011518339.3:c.3382A>G XP_011516641.1:p.Ile1128Val
XM_011518340.3:c.3382A>G XP_011516642.1:p.Ile1128Val
XM_011518341.3:c.3382A>G XP_011516643.1:p.Ile1128Val
XM_011518342.3:c.2944A>G XP_011516644.1:p.Ile982Val
XM_011518344.2:c.3382A>G XP_011516646.1:p.Ile1128Val
XM_017014378.2:c.3382A>G XP_016869867.1:p.Ile1128Val
XM_017014379.2:c.3382A>G XP_016869868.1:p.Ile1128Val
XM_017014380.2:c.3382A>G XP_016869869.1:p.Ile1128Val
XM_017014381.2:c.3382A>G XP_016869870.1:p.Ile1128Val
XM_017014382.2:c.3244A>G XP_016869871.1:p.Ile1082Val
XR_001746223.1:n.3695A>G
NM_005502.4:c.3307A>G MANE Select NP_005493.2:p.Ile1103Val