Canonical Allele Identifier: CA1869926515
Gene: ABCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.104832100_104832102delinsTTC , CM000671.2:g.104832100_104832102delinsTTC GRCh38
NC_000009.11:g.107594381_107594383delinsTTC , CM000671.1:g.107594381_107594383delinsTTC GRCh37
NC_000009.10:g.106634202_106634204delinsTTC NCBI36
NG_007981.1:g.101054_101056delinsGAA

Transcript Alleles

HGVS Amino-acid change
ENST00000374736.8:c.1510-275_1510-273delinsGAA MANE Select ENSP00000363868.3:n.1510-275_1510-273deli...
ENST00000678995.1:c.1510-275_1510-273delinsGAA ENSP00000504612.1:n.1510-275_1510-273deli...
ENST00000374736.7:c.1510-275_1510-273delinsGAA ENSP00000363868.3:n.1510-275_1510-273deli...
NM_005502.3:c.1510-275_1510-273delinsGAA NP_005493.2:n.1510-275_1510-273delinsGAA
XM_005251773.1:c.1510-275_1510-273delinsGAA XP_005251830.1:n.1510-275_1510-273delinsG...
XM_005251776.1:c.1330-275_1330-273delinsGAA XP_005251833.1:n.1330-275_1330-273delinsG...
XM_011518339.1:c.1585-275_1585-273delinsGAA XP_011516641.1:n.1585-275_1585-273delinsG...
XM_011518340.1:c.1585-275_1585-273delinsGAA XP_011516642.1:n.1585-275_1585-273delinsG...
XM_011518341.1:c.1585-275_1585-273delinsGAA XP_011516643.1:n.1585-275_1585-273delinsG...
XM_011518342.1:c.1147-275_1147-273delinsGAA XP_011516644.1:n.1147-275_1147-273delinsG...
XM_011518343.1:c.1585-275_1585-273delinsGAA XP_011516645.1:n.1585-275_1585-273delinsG...
XM_011518344.1:c.1585-275_1585-273delinsGAA XP_011516646.1:n.1585-275_1585-273delinsG...
XM_005251773.3:c.1510-275_1510-273delinsGAA XP_005251830.1:n.1510-275_1510-273delinsG...
XM_005251776.3:c.1330-275_1330-273delinsGAA XP_005251833.1:n.1330-275_1330-273delinsG...
XM_011518339.3:c.1585-275_1585-273delinsGAA XP_011516641.1:n.1585-275_1585-273delinsG...
XM_011518340.3:c.1585-275_1585-273delinsGAA XP_011516642.1:n.1585-275_1585-273delinsG...
XM_011518341.3:c.1585-275_1585-273delinsGAA XP_011516643.1:n.1585-275_1585-273delinsG...
XM_011518342.3:c.1147-275_1147-273delinsGAA XP_011516644.1:n.1147-275_1147-273delinsG...
XM_011518344.2:c.1585-275_1585-273delinsGAA XP_011516646.1:n.1585-275_1585-273delinsG...
XM_017014378.2:c.1585-275_1585-273delinsGAA XP_016869867.1:n.1585-275_1585-273delinsG...
XM_017014379.2:c.1585-275_1585-273delinsGAA XP_016869868.1:n.1585-275_1585-273delinsG...
XM_017014380.2:c.1585-275_1585-273delinsGAA XP_016869869.1:n.1585-275_1585-273delinsG...
XM_017014381.2:c.1585-275_1585-273delinsGAA XP_016869870.1:n.1585-275_1585-273delinsG...
XM_017014382.2:c.1447-275_1447-273delinsGAA XP_016869871.1:n.1447-275_1447-273delinsG...
XR_001746223.1:n.1898-275_1898-273delinsGAA
NM_005502.4:c.1510-275_1510-273delinsGAA MANE Select NP_005493.2:n.1510-275_1510-273delinsGAA