Canonical Allele Identifier: CA374322229

Gene: ABCA1

Linked Data

• dbSNP Id: rs1388254764
• gnomAD v4: 9-104829018-C-T
• MyVariant Identifiers: chr9:g.107591299C>T (hg19) ; chr9:g.104829018C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.104829018C>T , CM000671.2:g.104829018C>T	GRCh38
NC_000009.11:g.107591299C>T , CM000671.1:g.107591299C>T	GRCh37
NC_000009.10:g.106631120C>T	NCBI36
NG_007981.1:g.104138G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374736.8:c.2013G>A MANE Select	ENSP00000363868.3:p.Met671Ile
ENST00000678995.1:c.2013G>A	ENSP00000504612.1:p.Met671Ile
ENST00000374736.7:c.2013G>A	ENSP00000363868.3:p.Met671Ile
ENST00000494467.1:n.186G>A
NM_005502.3:c.2013G>A	NP_005493.2:p.Met671Ile
XM_005251773.1:c.2013G>A	XP_005251830.1:p.Met671Ile
XM_005251776.1:c.1833G>A	XP_005251833.1:p.Met611Ile
XM_011518339.1:c.2088G>A	XP_011516641.1:p.Met696Ile
XM_011518340.1:c.2088G>A	XP_011516642.1:p.Met696Ile
XM_011518341.1:c.2088G>A	XP_011516643.1:p.Met696Ile
XM_011518342.1:c.1650G>A	XP_011516644.1:p.Met550Ile
XM_011518343.1:c.2088G>A	XP_011516645.1:p.Met696Ile
XM_011518344.1:c.2088G>A	XP_011516646.1:p.Met696Ile
XM_005251773.3:c.2013G>A	XP_005251830.1:p.Met671Ile
XM_005251776.3:c.1833G>A	XP_005251833.1:p.Met611Ile
XM_011518339.3:c.2088G>A	XP_011516641.1:p.Met696Ile
XM_011518340.3:c.2088G>A	XP_011516642.1:p.Met696Ile
XM_011518341.3:c.2088G>A	XP_011516643.1:p.Met696Ile
XM_011518342.3:c.1650G>A	XP_011516644.1:p.Met550Ile
XM_011518344.2:c.2088G>A	XP_011516646.1:p.Met696Ile
XM_017014378.2:c.2088G>A	XP_016869867.1:p.Met696Ile
XM_017014379.2:c.2088G>A	XP_016869868.1:p.Met696Ile
XM_017014380.2:c.2088G>A	XP_016869869.1:p.Met696Ile
XM_017014381.2:c.2088G>A	XP_016869870.1:p.Met696Ile
XM_017014382.2:c.1950G>A	XP_016869871.1:p.Met650Ile
XR_001746223.1:n.2401G>A
NM_005502.4:c.2013G>A MANE Select	NP_005493.2:p.Met671Ile