Canonical Allele Identifier: CA1869965105
Gene: ABCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.104928087G= , CM000671.2:g.104928087G= GRCh38
NC_000009.11:g.107690368G= , CM000671.1:g.107690368G= GRCh37
NC_000009.10:g.106730189G= NCBI36
NG_007981.1:g.5069C=

Transcript Alleles

HGVS Amino-acid change
ENST00000374736.8:c.-245C= MANE Select ENSP00000363868.3:n.-245C=
ENST00000678995.1:c.-245C= ENSP00000504612.1:n.-245C=
ENST00000374733.1:c.-267C= ENSP00000363865.1:n.-267C=
ENST00000374736.7:c.-245C= ENSP00000363868.3:n.-245C=
ENST00000423487.6:c.-245C= ENSP00000416623.2:n.-245C=
NM_005502.3:c.-245C= NP_005493.2:n.-245C=
XM_005251773.1:c.-245C= XP_005251830.1:n.-245C=
XM_005251776.1:c.-267C= XP_005251833.1:n.-267C=
XM_011518339.1:c.-245C= XP_011516641.1:n.-245C=
XM_011518341.1:c.-245C= XP_011516643.1:n.-245C=
XM_011518342.1:c.-308C= XP_011516644.1:n.-308C=
XM_011518343.1:c.-245C= XP_011516645.1:n.-245C=
XM_011518344.1:c.-245C= XP_011516646.1:n.-245C=
XR_930204.1:n.734+177G=
XM_005251773.3:c.-245C= XP_005251830.1:n.-245C=
XM_005251776.3:c.-267C= XP_005251833.1:n.-267C=
XM_011518339.3:c.-245C= XP_011516641.1:n.-245C=
XM_011518341.3:c.-245C= XP_011516643.1:n.-245C=
XM_011518342.3:c.-308C= XP_011516644.1:n.-308C=
XM_011518344.2:c.-245C= XP_011516646.1:n.-245C=
XR_001746223.1:n.69C=
XR_930204.2:n.115+177G=
NM_005502.4:c.-245C= MANE Select NP_005493.2:n.-245C=