Canonical Allele Identifier: CA1869959296
Gene: ABCA1 HGNC NCBI

Linked Data

dbSNP Id: rs1841761075

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.104915048C>A , CM000671.2:g.104915048C>A GRCh38
NC_000009.11:g.107677329C>A , CM000671.1:g.107677329C>A GRCh37
NC_000009.10:g.106717150C>A NCBI36
NG_007981.1:g.18108G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000374736.8:c.-92-11277G>T MANE Select ENSP00000363868.3:n.-92-11277G>T
ENST00000678995.1:c.-92-11277G>T ENSP00000504612.1:n.-92-11277G>T
ENST00000374733.1:c.-115+12887G>T ENSP00000363865.1:n.-115+12887G>T
ENST00000374736.7:c.-92-11277G>T ENSP00000363868.3:n.-92-11277G>T
ENST00000423487.6:c.-92-11277G>T ENSP00000416623.2:n.-92-11277G>T
NM_005502.3:c.-92-11277G>T NP_005493.2:n.-92-11277G>T
XM_005251773.1:c.-92-11277G>T XP_005251830.1:n.-92-11277G>T
XM_005251776.1:c.-115+12887G>T XP_005251833.1:n.-115+12887G>T
XM_011518339.1:c.-92-11277G>T XP_011516641.1:n.-92-11277G>T
XM_011518341.1:c.-92-11277G>T XP_011516643.1:n.-92-11277G>T
XM_011518342.1:c.-156+12887G>T XP_011516644.1:n.-156+12887G>T
XM_011518343.1:c.-92-11277G>T XP_011516645.1:n.-92-11277G>T
XM_011518344.1:c.-92-11277G>T XP_011516646.1:n.-92-11277G>T
XR_428585.2:n.999-3614C>A
XR_428586.2:n.999-3614C>A
XR_428587.2:n.20+2708C>A
XM_005251773.3:c.-92-11277G>T XP_005251830.1:n.-92-11277G>T
XM_005251776.3:c.-115+12887G>T XP_005251833.1:n.-115+12887G>T
XM_011518339.3:c.-92-11277G>T XP_011516641.1:n.-92-11277G>T
XM_011518341.3:c.-92-11277G>T XP_011516643.1:n.-92-11277G>T
XM_011518342.3:c.-156+12887G>T XP_011516644.1:n.-156+12887G>T
XM_011518344.2:c.-92-11277G>T XP_011516646.1:n.-92-11277G>T
XR_001746223.1:n.222-11277G>T
NM_005502.4:c.-92-11277G>T MANE Select NP_005493.2:n.-92-11277G>T