Canonical Allele Identifier: CA1869919905
Gene: ABCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.104828895G= , CM000671.2:g.104828895G= GRCh38
NC_000009.11:g.107591176G= , CM000671.1:g.107591176G= GRCh37
NC_000009.10:g.106630997G= NCBI36
NG_007981.1:g.104261C=

Transcript Alleles

HGVS Amino-acid change
ENST00000374736.8:c.2115+21C= MANE Select ENSP00000363868.3:n.2115+21C=
ENST00000678995.1:c.2115+21C= ENSP00000504612.1:n.2115+21C=
ENST00000374736.7:c.2115+21C= ENSP00000363868.3:n.2115+21C=
ENST00000494467.1:n.288+21C=
NM_005502.3:c.2115+21C= NP_005493.2:n.2115+21C=
XM_005251773.1:c.2115+21C= XP_005251830.1:n.2115+21C=
XM_005251776.1:c.1935+21C= XP_005251833.1:n.1935+21C=
XM_011518339.1:c.2190+21C= XP_011516641.1:n.2190+21C=
XM_011518340.1:c.2190+21C= XP_011516642.1:n.2190+21C=
XM_011518341.1:c.2190+21C= XP_011516643.1:n.2190+21C=
XM_011518342.1:c.1752+21C= XP_011516644.1:n.1752+21C=
XM_011518343.1:c.2190+21C= XP_011516645.1:n.2190+21C=
XM_011518344.1:c.2190+21C= XP_011516646.1:n.2190+21C=
XM_005251773.3:c.2115+21C= XP_005251830.1:n.2115+21C=
XM_005251776.3:c.1935+21C= XP_005251833.1:n.1935+21C=
XM_011518339.3:c.2190+21C= XP_011516641.1:n.2190+21C=
XM_011518340.3:c.2190+21C= XP_011516642.1:n.2190+21C=
XM_011518341.3:c.2190+21C= XP_011516643.1:n.2190+21C=
XM_011518342.3:c.1752+21C= XP_011516644.1:n.1752+21C=
XM_011518344.2:c.2190+21C= XP_011516646.1:n.2190+21C=
XM_017014378.2:c.2190+21C= XP_016869867.1:n.2190+21C=
XM_017014379.2:c.2190+21C= XP_016869868.1:n.2190+21C=
XM_017014380.2:c.2190+21C= XP_016869869.1:n.2190+21C=
XM_017014381.2:c.2190+21C= XP_016869870.1:n.2190+21C=
XM_017014382.2:c.2052+21C= XP_016869871.1:n.2052+21C=
XR_001746223.1:n.2503+21C=
NM_005502.4:c.2115+21C= MANE Select NP_005493.2:n.2115+21C=