Canonical Allele Identifier: CA2691057792
Gene: ABCA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.104928077C>A , CM000671.2:g.104928077C>A GRCh38
NC_000009.11:g.107690358C>A , CM000671.1:g.107690358C>A GRCh37
NC_000009.10:g.106730179C>A NCBI36
NG_007981.1:g.5079G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000374736.8:c.-235G>T MANE Select ENSP00000363868.3:n.-235G>T
ENST00000678995.1:c.-235G>T ENSP00000504612.1:n.-235G>T
ENST00000374733.1:c.-257G>T ENSP00000363865.1:n.-257G>T
ENST00000374736.7:c.-235G>T ENSP00000363868.3:n.-235G>T
ENST00000423487.6:c.-235G>T ENSP00000416623.2:n.-235G>T
NM_005502.3:c.-235G>T NP_005493.2:n.-235G>T
XM_005251773.1:c.-235G>T XP_005251830.1:n.-235G>T
XM_005251776.1:c.-257G>T XP_005251833.1:n.-257G>T
XM_011518339.1:c.-235G>T XP_011516641.1:n.-235G>T
XM_011518341.1:c.-235G>T XP_011516643.1:n.-235G>T
XM_011518342.1:c.-298G>T XP_011516644.1:n.-298G>T
XM_011518343.1:c.-235G>T XP_011516645.1:n.-235G>T
XM_011518344.1:c.-235G>T XP_011516646.1:n.-235G>T
XR_930204.1:n.734+167C>A
XM_005251773.3:c.-235G>T XP_005251830.1:n.-235G>T
XM_005251776.3:c.-257G>T XP_005251833.1:n.-257G>T
XM_011518339.3:c.-235G>T XP_011516641.1:n.-235G>T
XM_011518341.3:c.-235G>T XP_011516643.1:n.-235G>T
XM_011518342.3:c.-298G>T XP_011516644.1:n.-298G>T
XM_011518344.2:c.-235G>T XP_011516646.1:n.-235G>T
XR_001746223.1:n.79G>T
XR_930204.2:n.115+167C>A
NM_005502.4:c.-235G>T MANE Select NP_005493.2:n.-235G>T