Canonical Allele Identifier: CA1869965096
Gene: ABCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.104928071C= , CM000671.2:g.104928071C= GRCh38
NC_000009.11:g.107690352C= , CM000671.1:g.107690352C= GRCh37
NC_000009.10:g.106730173C= NCBI36
NG_007981.1:g.5085G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374736.8:c.-229G= MANE Select ENSP00000363868.3:n.-229G=
ENST00000678995.1:c.-229G= ENSP00000504612.1:n.-229G=
ENST00000374733.1:c.-251G= ENSP00000363865.1:n.-251G=
ENST00000374736.7:c.-229G= ENSP00000363868.3:n.-229G=
ENST00000423487.6:c.-229G= ENSP00000416623.2:n.-229G=
NM_005502.3:c.-229G= NP_005493.2:n.-229G=
XM_005251773.1:c.-229G= XP_005251830.1:n.-229G=
XM_005251776.1:c.-251G= XP_005251833.1:n.-251G=
XM_011518339.1:c.-229G= XP_011516641.1:n.-229G=
XM_011518341.1:c.-229G= XP_011516643.1:n.-229G=
XM_011518342.1:c.-292G= XP_011516644.1:n.-292G=
XM_011518343.1:c.-229G= XP_011516645.1:n.-229G=
XM_011518344.1:c.-229G= XP_011516646.1:n.-229G=
XR_930204.1:n.734+161C=
XM_005251773.3:c.-229G= XP_005251830.1:n.-229G=
XM_005251776.3:c.-251G= XP_005251833.1:n.-251G=
XM_011518339.3:c.-229G= XP_011516641.1:n.-229G=
XM_011518341.3:c.-229G= XP_011516643.1:n.-229G=
XM_011518342.3:c.-292G= XP_011516644.1:n.-292G=
XM_011518344.2:c.-229G= XP_011516646.1:n.-229G=
XR_001746223.1:n.85G=
XR_930204.2:n.115+161C=
NM_005502.4:c.-229G= MANE Select NP_005493.2:n.-229G=