Canonical Allele Identifier: CA374314090

Gene: ABCA1

Linked Data

• MyVariant Identifiers: chr9:g.107560785G>C (hg19) ; chr9:g.104798504G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.104798504G>C , CM000671.2:g.104798504G>C	GRCh38
NC_000009.11:g.107560785G>C , CM000671.1:g.107560785G>C	GRCh37
NC_000009.10:g.106600606G>C	NCBI36
NG_007981.1:g.134652C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000374736.8:c.5038C>G MANE Select	ENSP00000363868.3:p.Arg1680Gly
ENST00000678995.1:c.5044C>G	ENSP00000504612.1:p.Arg1682Gly
ENST00000374736.7:c.5038C>G	ENSP00000363868.3:p.Arg1680Gly
NM_005502.3:c.5038C>G	NP_005493.2:p.Arg1680Gly
XM_005251773.1:c.5044C>G	XP_005251830.1:p.Arg1682Gly
XM_005251776.1:c.4864C>G	XP_005251833.1:p.Arg1622Gly
XM_011518339.1:c.5119C>G	XP_011516641.1:p.Arg1707Gly
XM_011518340.1:c.5119C>G	XP_011516642.1:p.Arg1707Gly
XM_011518341.1:c.5113C>G	XP_011516643.1:p.Arg1705Gly
XM_011518342.1:c.4681C>G	XP_011516644.1:p.Arg1561Gly
XM_011518343.1:c.5119C>G	XP_011516645.1:p.Arg1707Gly
XM_005251773.3:c.5044C>G	XP_005251830.1:p.Arg1682Gly
XM_005251776.3:c.4864C>G	XP_005251833.1:p.Arg1622Gly
XM_011518339.3:c.5119C>G	XP_011516641.1:p.Arg1707Gly
XM_011518340.3:c.5119C>G	XP_011516642.1:p.Arg1707Gly
XM_011518341.3:c.5113C>G	XP_011516643.1:p.Arg1705Gly
XM_011518342.3:c.4681C>G	XP_011516644.1:p.Arg1561Gly
XM_017014378.2:c.5119C>G	XP_016869867.1:p.Arg1707Gly
XM_017014379.2:c.5119C>G	XP_016869868.1:p.Arg1707Gly
XM_017014380.2:c.5119C>G	XP_016869869.1:p.Arg1707Gly
XM_017014381.2:c.5119C>G	XP_016869870.1:p.Arg1707Gly
XM_017014382.2:c.4981C>G	XP_016869871.1:p.Arg1661Gly
XR_001746223.1:n.5432C>G
NM_005502.4:c.5038C>G MANE Select	NP_005493.2:p.Arg1680Gly