Canonical Allele Identifier: CA374314128

Gene: ABCA1

Linked Data

• dbSNP Id: rs1353120003
• gnomAD v4: 9-104798521-A-G
• MyVariant Identifiers: chr9:g.107560802A>G (hg19) ; chr9:g.104798521A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.104798521A>G , CM000671.2:g.104798521A>G	GRCh38
NC_000009.11:g.107560802A>G , CM000671.1:g.107560802A>G	GRCh37
NC_000009.10:g.106600623A>G	NCBI36
NG_007981.1:g.134635T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374736.8:c.5021T>C MANE Select	ENSP00000363868.3:p.Val1674Ala
ENST00000678995.1:c.5027T>C	ENSP00000504612.1:p.Val1676Ala
ENST00000374736.7:c.5021T>C	ENSP00000363868.3:p.Val1674Ala
NM_005502.3:c.5021T>C	NP_005493.2:p.Val1674Ala
XM_005251773.1:c.5027T>C	XP_005251830.1:p.Val1676Ala
XM_005251776.1:c.4847T>C	XP_005251833.1:p.Val1616Ala
XM_011518339.1:c.5102T>C	XP_011516641.1:p.Val1701Ala
XM_011518340.1:c.5102T>C	XP_011516642.1:p.Val1701Ala
XM_011518341.1:c.5096T>C	XP_011516643.1:p.Val1699Ala
XM_011518342.1:c.4664T>C	XP_011516644.1:p.Val1555Ala
XM_011518343.1:c.5102T>C	XP_011516645.1:p.Val1701Ala
XM_005251773.3:c.5027T>C	XP_005251830.1:p.Val1676Ala
XM_005251776.3:c.4847T>C	XP_005251833.1:p.Val1616Ala
XM_011518339.3:c.5102T>C	XP_011516641.1:p.Val1701Ala
XM_011518340.3:c.5102T>C	XP_011516642.1:p.Val1701Ala
XM_011518341.3:c.5096T>C	XP_011516643.1:p.Val1699Ala
XM_011518342.3:c.4664T>C	XP_011516644.1:p.Val1555Ala
XM_017014378.2:c.5102T>C	XP_016869867.1:p.Val1701Ala
XM_017014379.2:c.5102T>C	XP_016869868.1:p.Val1701Ala
XM_017014380.2:c.5102T>C	XP_016869869.1:p.Val1701Ala
XM_017014381.2:c.5102T>C	XP_016869870.1:p.Val1701Ala
XM_017014382.2:c.4964T>C	XP_016869871.1:p.Val1655Ala
XR_001746223.1:n.5415T>C
NM_005502.4:c.5021T>C MANE Select	NP_005493.2:p.Val1674Ala