Canonical Allele Identifier: CA466500913
Gene: ABCA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.107553208T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.104790927T>C , CM000671.2:g.104790927T>C GRCh38
NC_000009.11:g.107553208T>C , CM000671.1:g.107553208T>C GRCh37
NC_000009.10:g.106593029T>C NCBI36
NG_007981.1:g.142229A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000374736.8:c.5922A>G MANE Select ENSP00000363868.3:p.Lys1974=
ENST00000678995.1:c.5928A>G ENSP00000504612.1:p.Lys1976=
ENST00000374736.7:c.5922A>G ENSP00000363868.3:p.Lys1974=
NM_005502.3:c.5922A>G NP_005493.2:p.Lys1974=
XM_005251773.1:c.5928A>G XP_005251830.1:p.Lys1976=
XM_005251776.1:c.5748A>G XP_005251833.1:p.Lys1916=
XM_011518339.1:c.6003A>G XP_011516641.1:p.Lys2001=
XM_011518340.1:c.6003A>G XP_011516642.1:p.Lys2001=
XM_011518341.1:c.5997A>G XP_011516643.1:p.Lys1999=
XM_011518342.1:c.5565A>G XP_011516644.1:p.Lys1855=
XM_011518343.1:c.6003A>G XP_011516645.1:p.Lys2001=
XM_005251773.3:c.5928A>G XP_005251830.1:p.Lys1976=
XM_005251776.3:c.5748A>G XP_005251833.1:p.Lys1916=
XM_011518339.3:c.6003A>G XP_011516641.1:p.Lys2001=
XM_011518340.3:c.6003A>G XP_011516642.1:p.Lys2001=
XM_011518341.3:c.5997A>G XP_011516643.1:p.Lys1999=
XM_011518342.3:c.5565A>G XP_011516644.1:p.Lys1855=
XM_017014378.2:c.6003A>G XP_016869867.1:p.Lys2001=
XM_017014379.2:c.6003A>G XP_016869868.1:p.Lys2001=
XM_017014380.2:c.6003A>G XP_016869869.1:p.Lys2001=
XM_017014381.2:c.6003A>G XP_016869870.1:p.Lys2001=
XM_017014382.2:c.5865A>G XP_016869871.1:p.Lys1955=
XR_001746223.1:n.6316A>G
NM_005502.4:c.5922A>G MANE Select NP_005493.2:p.Lys1974=