Canonical Allele Identifier: CA466502268

Gene: ABCA1

Linked Data

• gnomAD v4: 9-104884456-G-C
• MyVariant Identifiers: chr9:g.107646737G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.104884456G>C , CM000671.2:g.104884456G>C	GRCh38
NC_000009.11:g.107646737G>C , CM000671.1:g.107646737G>C	GRCh37
NC_000009.10:g.106686558G>C	NCBI36
NG_007981.1:g.48700C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374736.8:c.273C>G MANE Select	ENSP00000363868.3:p.Pro91=
ENST00000678995.1:c.273C>G	ENSP00000504612.1:p.Pro91=
ENST00000374733.1:c.93C>G	ENSP00000363865.1:p.Pro31=
ENST00000374736.7:c.273C>G	ENSP00000363868.3:p.Pro91=
ENST00000423487.6:c.273C>G	ENSP00000416623.2:p.Pro91=
NM_005502.3:c.273C>G	NP_005493.2:p.Pro91=
XM_005251773.1:c.273C>G	XP_005251830.1:p.Pro91=
XM_005251776.1:c.93C>G	XP_005251833.1:p.Pro31=
XM_011518339.1:c.348C>G	XP_011516641.1:p.Pro116=
XM_011518340.1:c.348C>G	XP_011516642.1:p.Pro116=
XM_011518341.1:c.348C>G	XP_011516643.1:p.Pro116=
XM_011518342.1:c.-61-1299C>G	XP_011516644.1:n.-61-1299C>G
XM_011518343.1:c.348C>G	XP_011516645.1:p.Pro116=
XM_011518344.1:c.348C>G	XP_011516646.1:p.Pro116=
XM_005251773.3:c.273C>G	XP_005251830.1:p.Pro91=
XM_005251776.3:c.93C>G	XP_005251833.1:p.Pro31=
XM_011518339.3:c.348C>G	XP_011516641.1:p.Pro116=
XM_011518340.3:c.348C>G	XP_011516642.1:p.Pro116=
XM_011518341.3:c.348C>G	XP_011516643.1:p.Pro116=
XM_011518342.3:c.-61-1299C>G	XP_011516644.1:n.-61-1299C>G
XM_011518344.2:c.348C>G	XP_011516646.1:p.Pro116=
XM_017014378.2:c.348C>G	XP_016869867.1:p.Pro116=
XM_017014379.2:c.348C>G	XP_016869868.1:p.Pro116=
XM_017014380.2:c.348C>G	XP_016869869.1:p.Pro116=
XM_017014381.2:c.348C>G	XP_016869870.1:p.Pro116=
XM_017014382.2:c.210C>G	XP_016869871.1:p.Pro70=
XR_001746223.1:n.661C>G
NM_005502.4:c.273C>G MANE Select	NP_005493.2:p.Pro91=