Canonical Allele Identifier: CA5168767
Gene: ABCA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 364433
dbSNP Id: rs2066718

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.104826974C>T , CM000671.2:g.104826974C>T GRCh38
NC_000009.11:g.107589255C>T , CM000671.1:g.107589255C>T GRCh37
NC_000009.10:g.106629076C>T NCBI36
NG_007981.1:g.106182G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000374736.8:c.2311G>A MANE Select ENSP00000363868.3:p.Val771Met
ENST00000678995.1:c.2311G>A ENSP00000504612.1:p.Val771Met
ENST00000374736.7:c.2311G>A ENSP00000363868.3:p.Val771Met
ENST00000494467.1:n.484G>A
NM_005502.3:c.2311G>A NP_005493.2:p.Val771Met
XM_005251773.1:c.2311G>A XP_005251830.1:p.Val771Met
XM_005251776.1:c.2131G>A XP_005251833.1:p.Val711Met
XM_011518339.1:c.2386G>A XP_011516641.1:p.Val796Met
XM_011518340.1:c.2386G>A XP_011516642.1:p.Val796Met
XM_011518341.1:c.2386G>A XP_011516643.1:p.Val796Met
XM_011518342.1:c.1948G>A XP_011516644.1:p.Val650Met
XM_011518343.1:c.2386G>A XP_011516645.1:p.Val796Met
XM_011518344.1:c.2386G>A XP_011516646.1:p.Val796Met
XM_005251773.3:c.2311G>A XP_005251830.1:p.Val771Met
XM_005251776.3:c.2131G>A XP_005251833.1:p.Val711Met
XM_011518339.3:c.2386G>A XP_011516641.1:p.Val796Met
XM_011518340.3:c.2386G>A XP_011516642.1:p.Val796Met
XM_011518341.3:c.2386G>A XP_011516643.1:p.Val796Met
XM_011518342.3:c.1948G>A XP_011516644.1:p.Val650Met
XM_011518344.2:c.2386G>A XP_011516646.1:p.Val796Met
XM_017014378.2:c.2386G>A XP_016869867.1:p.Val796Met
XM_017014379.2:c.2386G>A XP_016869868.1:p.Val796Met
XM_017014380.2:c.2386G>A XP_016869869.1:p.Val796Met
XM_017014381.2:c.2386G>A XP_016869870.1:p.Val796Met
XM_017014382.2:c.2248G>A XP_016869871.1:p.Val750Met
XR_001746223.1:n.2699G>A
NM_005502.4:c.2311G>A MANE Select NP_005493.2:p.Val771Met