Canonical Allele Identifier: CA858068388

Gene: ABCA1

Linked Data

• dbSNP Id: rs929902273
• MyVariant Identifiers: chr9:g.107647235G>C (hg19) ; chr9:g.104884954G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.104884954G>C , CM000671.2:g.104884954G>C	GRCh38
NC_000009.11:g.107647235G>C , CM000671.1:g.107647235G>C	GRCh37
NC_000009.10:g.106687056G>C	NCBI36
NG_007981.1:g.48202C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000374736.8:c.161-386C>G MANE Select	ENSP00000363868.3:n.161-386C>G
ENST00000678995.1:c.161-386C>G	ENSP00000504612.1:n.161-386C>G
ENST00000374733.1:c.-20-386C>G	ENSP00000363865.1:n.-20-386C>G
ENST00000374736.7:c.161-386C>G	ENSP00000363868.3:n.161-386C>G
ENST00000423487.6:c.161-386C>G	ENSP00000416623.2:n.161-386C>G
NM_005502.3:c.161-386C>G	NP_005493.2:n.161-386C>G
XM_005251773.1:c.161-386C>G	XP_005251830.1:n.161-386C>G
XM_005251776.1:c.-20-386C>G	XP_005251833.1:n.-20-386C>G
XM_011518339.1:c.236-386C>G	XP_011516641.1:n.236-386C>G
XM_011518340.1:c.236-386C>G	XP_011516642.1:n.236-386C>G
XM_011518341.1:c.236-386C>G	XP_011516643.1:n.236-386C>G
XM_011518342.1:c.-61-1797C>G	XP_011516644.1:n.-61-1797C>G
XM_011518343.1:c.236-386C>G	XP_011516645.1:n.236-386C>G
XM_011518344.1:c.236-386C>G	XP_011516646.1:n.236-386C>G
XM_005251773.3:c.161-386C>G	XP_005251830.1:n.161-386C>G
XM_005251776.3:c.-20-386C>G	XP_005251833.1:n.-20-386C>G
XM_011518339.3:c.236-386C>G	XP_011516641.1:n.236-386C>G
XM_011518340.3:c.236-386C>G	XP_011516642.1:n.236-386C>G
XM_011518341.3:c.236-386C>G	XP_011516643.1:n.236-386C>G
XM_011518342.3:c.-61-1797C>G	XP_011516644.1:n.-61-1797C>G
XM_011518344.2:c.236-386C>G	XP_011516646.1:n.236-386C>G
XM_017014378.2:c.236-386C>G	XP_016869867.1:n.236-386C>G
XM_017014379.2:c.236-386C>G	XP_016869868.1:n.236-386C>G
XM_017014380.2:c.236-386C>G	XP_016869869.1:n.236-386C>G
XM_017014381.2:c.236-386C>G	XP_016869870.1:n.236-386C>G
XM_017014382.2:c.98-386C>G	XP_016869871.1:n.98-386C>G
XR_001746223.1:n.549-386C>G
NM_005502.4:c.161-386C>G MANE Select	NP_005493.2:n.161-386C>G