Canonical Allele Identifier: CA374314137

Gene: ABCA1

Linked Data

• MyVariant Identifiers: chr9:g.107560806C>T (hg19) ; chr9:g.104798525C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.104798525C>T , CM000671.2:g.104798525C>T	GRCh38
NC_000009.11:g.107560806C>T , CM000671.1:g.107560806C>T	GRCh37
NC_000009.10:g.106600627C>T	NCBI36
NG_007981.1:g.134631G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374736.8:c.5017G>A MANE Select	ENSP00000363868.3:p.Val1673Ile
ENST00000678995.1:c.5023G>A	ENSP00000504612.1:p.Val1675Ile
ENST00000374736.7:c.5017G>A	ENSP00000363868.3:p.Val1673Ile
NM_005502.3:c.5017G>A	NP_005493.2:p.Val1673Ile
XM_005251773.1:c.5023G>A	XP_005251830.1:p.Val1675Ile
XM_005251776.1:c.4843G>A	XP_005251833.1:p.Val1615Ile
XM_011518339.1:c.5098G>A	XP_011516641.1:p.Val1700Ile
XM_011518340.1:c.5098G>A	XP_011516642.1:p.Val1700Ile
XM_011518341.1:c.5092G>A	XP_011516643.1:p.Val1698Ile
XM_011518342.1:c.4660G>A	XP_011516644.1:p.Val1554Ile
XM_011518343.1:c.5098G>A	XP_011516645.1:p.Val1700Ile
XM_005251773.3:c.5023G>A	XP_005251830.1:p.Val1675Ile
XM_005251776.3:c.4843G>A	XP_005251833.1:p.Val1615Ile
XM_011518339.3:c.5098G>A	XP_011516641.1:p.Val1700Ile
XM_011518340.3:c.5098G>A	XP_011516642.1:p.Val1700Ile
XM_011518341.3:c.5092G>A	XP_011516643.1:p.Val1698Ile
XM_011518342.3:c.4660G>A	XP_011516644.1:p.Val1554Ile
XM_017014378.2:c.5098G>A	XP_016869867.1:p.Val1700Ile
XM_017014379.2:c.5098G>A	XP_016869868.1:p.Val1700Ile
XM_017014380.2:c.5098G>A	XP_016869869.1:p.Val1700Ile
XM_017014381.2:c.5098G>A	XP_016869870.1:p.Val1700Ile
XM_017014382.2:c.4960G>A	XP_016869871.1:p.Val1654Ile
XR_001746223.1:n.5411G>A
NM_005502.4:c.5017G>A MANE Select	NP_005493.2:p.Val1673Ile