Canonical Allele Identifier: CA374314116
Gene: ABCA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.104798515A>T , CM000671.2:g.104798515A>T GRCh38
NC_000009.11:g.107560796A>T , CM000671.1:g.107560796A>T GRCh37
NC_000009.10:g.106600617A>T NCBI36
NG_007981.1:g.134641T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000374736.8:c.5027T>A MANE Select ENSP00000363868.3:p.Leu1676Gln
ENST00000678995.1:c.5033T>A ENSP00000504612.1:p.Leu1678Gln
ENST00000374736.7:c.5027T>A ENSP00000363868.3:p.Leu1676Gln
NM_005502.3:c.5027T>A NP_005493.2:p.Leu1676Gln
XM_005251773.1:c.5033T>A XP_005251830.1:p.Leu1678Gln
XM_005251776.1:c.4853T>A XP_005251833.1:p.Leu1618Gln
XM_011518339.1:c.5108T>A XP_011516641.1:p.Leu1703Gln
XM_011518340.1:c.5108T>A XP_011516642.1:p.Leu1703Gln
XM_011518341.1:c.5102T>A XP_011516643.1:p.Leu1701Gln
XM_011518342.1:c.4670T>A XP_011516644.1:p.Leu1557Gln
XM_011518343.1:c.5108T>A XP_011516645.1:p.Leu1703Gln
XM_005251773.3:c.5033T>A XP_005251830.1:p.Leu1678Gln
XM_005251776.3:c.4853T>A XP_005251833.1:p.Leu1618Gln
XM_011518339.3:c.5108T>A XP_011516641.1:p.Leu1703Gln
XM_011518340.3:c.5108T>A XP_011516642.1:p.Leu1703Gln
XM_011518341.3:c.5102T>A XP_011516643.1:p.Leu1701Gln
XM_011518342.3:c.4670T>A XP_011516644.1:p.Leu1557Gln
XM_017014378.2:c.5108T>A XP_016869867.1:p.Leu1703Gln
XM_017014379.2:c.5108T>A XP_016869868.1:p.Leu1703Gln
XM_017014380.2:c.5108T>A XP_016869869.1:p.Leu1703Gln
XM_017014381.2:c.5108T>A XP_016869870.1:p.Leu1703Gln
XM_017014382.2:c.4970T>A XP_016869871.1:p.Leu1657Gln
XR_001746223.1:n.5421T>A
NM_005502.4:c.5027T>A MANE Select NP_005493.2:p.Leu1676Gln