Canonical Allele Identifier: CA374314227

Gene: ABCA1

Linked Data

• dbSNP Id: rs1182108398
• MyVariant Identifiers: chr9:g.107560847A>G (hg19) ; chr9:g.104798566A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.104798566A>G , CM000671.2:g.104798566A>G	GRCh38
NC_000009.11:g.107560847A>G , CM000671.1:g.107560847A>G	GRCh37
NC_000009.10:g.106600668A>G	NCBI36
NG_007981.1:g.134590T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374736.8:c.4976T>C MANE Select	ENSP00000363868.3:p.Ile1659Thr
ENST00000678995.1:c.4982T>C	ENSP00000504612.1:p.Ile1661Thr
ENST00000374736.7:c.4976T>C	ENSP00000363868.3:p.Ile1659Thr
NM_005502.3:c.4976T>C	NP_005493.2:p.Ile1659Thr
XM_005251773.1:c.4982T>C	XP_005251830.1:p.Ile1661Thr
XM_005251776.1:c.4802T>C	XP_005251833.1:p.Ile1601Thr
XM_011518339.1:c.5057T>C	XP_011516641.1:p.Ile1686Thr
XM_011518340.1:c.5057T>C	XP_011516642.1:p.Ile1686Thr
XM_011518341.1:c.5051T>C	XP_011516643.1:p.Ile1684Thr
XM_011518342.1:c.4619T>C	XP_011516644.1:p.Ile1540Thr
XM_011518343.1:c.5057T>C	XP_011516645.1:p.Ile1686Thr
XM_005251773.3:c.4982T>C	XP_005251830.1:p.Ile1661Thr
XM_005251776.3:c.4802T>C	XP_005251833.1:p.Ile1601Thr
XM_011518339.3:c.5057T>C	XP_011516641.1:p.Ile1686Thr
XM_011518340.3:c.5057T>C	XP_011516642.1:p.Ile1686Thr
XM_011518341.3:c.5051T>C	XP_011516643.1:p.Ile1684Thr
XM_011518342.3:c.4619T>C	XP_011516644.1:p.Ile1540Thr
XM_017014378.2:c.5057T>C	XP_016869867.1:p.Ile1686Thr
XM_017014379.2:c.5057T>C	XP_016869868.1:p.Ile1686Thr
XM_017014380.2:c.5057T>C	XP_016869869.1:p.Ile1686Thr
XM_017014381.2:c.5057T>C	XP_016869870.1:p.Ile1686Thr
XM_017014382.2:c.4919T>C	XP_016869871.1:p.Ile1640Thr
XR_001746223.1:n.5370T>C
NM_005502.4:c.4976T>C MANE Select	NP_005493.2:p.Ile1659Thr