Canonical Allele Identifier: CA1869919886
Gene: ABCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.104828879_104828880delinsGT , CM000671.2:g.104828879_104828880delinsGT GRCh38
NC_000009.11:g.107591160_107591161delinsGT , CM000671.1:g.107591160_107591161delinsGT GRCh37
NC_000009.10:g.106630981_106630982delinsGT NCBI36
NG_007981.1:g.104276_104277delinsAC

Transcript Alleles

HGVS Amino-acid change
ENST00000374736.8:c.2115+36_2115+37delinsAC MANE Select ENSP00000363868.3:n.2115+36_2115+37delins...
ENST00000678995.1:c.2115+36_2115+37delinsAC ENSP00000504612.1:n.2115+36_2115+37delins...
ENST00000374736.7:c.2115+36_2115+37delinsAC ENSP00000363868.3:n.2115+36_2115+37delins...
ENST00000494467.1:n.288+36_288+37delinsAC
NM_005502.3:c.2115+36_2115+37delinsAC NP_005493.2:n.2115+36_2115+37delinsAC
XM_005251773.1:c.2115+36_2115+37delinsAC XP_005251830.1:n.2115+36_2115+37delinsAC
XM_005251776.1:c.1935+36_1935+37delinsAC XP_005251833.1:n.1935+36_1935+37delinsAC
XM_011518339.1:c.2190+36_2190+37delinsAC XP_011516641.1:n.2190+36_2190+37delinsAC
XM_011518340.1:c.2190+36_2190+37delinsAC XP_011516642.1:n.2190+36_2190+37delinsAC
XM_011518341.1:c.2190+36_2190+37delinsAC XP_011516643.1:n.2190+36_2190+37delinsAC
XM_011518342.1:c.1752+36_1752+37delinsAC XP_011516644.1:n.1752+36_1752+37delinsAC
XM_011518343.1:c.2190+36_2190+37delinsAC XP_011516645.1:n.2190+36_2190+37delinsAC
XM_011518344.1:c.2190+36_2190+37delinsAC XP_011516646.1:n.2190+36_2190+37delinsAC
XM_005251773.3:c.2115+36_2115+37delinsAC XP_005251830.1:n.2115+36_2115+37delinsAC
XM_005251776.3:c.1935+36_1935+37delinsAC XP_005251833.1:n.1935+36_1935+37delinsAC
XM_011518339.3:c.2190+36_2190+37delinsAC XP_011516641.1:n.2190+36_2190+37delinsAC
XM_011518340.3:c.2190+36_2190+37delinsAC XP_011516642.1:n.2190+36_2190+37delinsAC
XM_011518341.3:c.2190+36_2190+37delinsAC XP_011516643.1:n.2190+36_2190+37delinsAC
XM_011518342.3:c.1752+36_1752+37delinsAC XP_011516644.1:n.1752+36_1752+37delinsAC
XM_011518344.2:c.2190+36_2190+37delinsAC XP_011516646.1:n.2190+36_2190+37delinsAC
XM_017014378.2:c.2190+36_2190+37delinsAC XP_016869867.1:n.2190+36_2190+37delinsAC
XM_017014379.2:c.2190+36_2190+37delinsAC XP_016869868.1:n.2190+36_2190+37delinsAC
XM_017014380.2:c.2190+36_2190+37delinsAC XP_016869869.1:n.2190+36_2190+37delinsAC
XM_017014381.2:c.2190+36_2190+37delinsAC XP_016869870.1:n.2190+36_2190+37delinsAC
XM_017014382.2:c.2052+36_2052+37delinsAC XP_016869871.1:n.2052+36_2052+37delinsAC
XR_001746223.1:n.2503+36_2503+37delinsAC
NM_005502.4:c.2115+36_2115+37delinsAC MANE Select NP_005493.2:n.2115+36_2115+37delinsAC