Canonical Allele Identifier: CA466506705
Gene: ABCA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.107584815G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.104822534G>A , CM000671.2:g.104822534G>A GRCh38
NC_000009.11:g.107584815G>A , CM000671.1:g.107584815G>A GRCh37
NC_000009.10:g.106624636G>A NCBI36
NG_007981.1:g.110622C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000374736.8:c.2790C>T MANE Select ENSP00000363868.3:p.Ser930=
ENST00000678995.1:c.2790C>T ENSP00000504612.1:p.Ser930=
ENST00000374736.7:c.2790C>T ENSP00000363868.3:p.Ser930=
NM_005502.3:c.2790C>T NP_005493.2:p.Ser930=
XM_005251773.1:c.2790C>T XP_005251830.1:p.Ser930=
XM_005251776.1:c.2610C>T XP_005251833.1:p.Ser870=
XM_011518339.1:c.2865C>T XP_011516641.1:p.Ser955=
XM_011518340.1:c.2865C>T XP_011516642.1:p.Ser955=
XM_011518341.1:c.2865C>T XP_011516643.1:p.Ser955=
XM_011518342.1:c.2427C>T XP_011516644.1:p.Ser809=
XM_011518343.1:c.2865C>T XP_011516645.1:p.Ser955=
XM_011518344.1:c.2865C>T XP_011516646.1:p.Ser955=
XM_005251773.3:c.2790C>T XP_005251830.1:p.Ser930=
XM_005251776.3:c.2610C>T XP_005251833.1:p.Ser870=
XM_011518339.3:c.2865C>T XP_011516641.1:p.Ser955=
XM_011518340.3:c.2865C>T XP_011516642.1:p.Ser955=
XM_011518341.3:c.2865C>T XP_011516643.1:p.Ser955=
XM_011518342.3:c.2427C>T XP_011516644.1:p.Ser809=
XM_011518344.2:c.2865C>T XP_011516646.1:p.Ser955=
XM_017014378.2:c.2865C>T XP_016869867.1:p.Ser955=
XM_017014379.2:c.2865C>T XP_016869868.1:p.Ser955=
XM_017014380.2:c.2865C>T XP_016869869.1:p.Ser955=
XM_017014381.2:c.2865C>T XP_016869870.1:p.Ser955=
XM_017014382.2:c.2727C>T XP_016869871.1:p.Ser909=
XR_001746223.1:n.3178C>T
NM_005502.4:c.2790C>T MANE Select NP_005493.2:p.Ser930=