Canonical Allele Identifier: CA2691055902
Gene: ABCA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.104826900_104826910del , CM000671.2:g.104826900_104826910del GRCh38
NC_000009.11:g.107589181_107589191del , CM000671.1:g.107589181_107589191del GRCh37
NC_000009.10:g.106629002_106629012del NCBI36
NG_007981.1:g.106250_106260del

Transcript Alleles

HGVS Amino-acid change
ENST00000374736.8:c.2337+42_2337+52del MANE Select ENSP00000363868.3:n.2337+42_2337+52del
ENST00000678995.1:c.2337+42_2337+52del ENSP00000504612.1:n.2337+42_2337+52del
ENST00000374736.7:c.2337+42_2337+52del ENSP00000363868.3:n.2337+42_2337+52del
ENST00000494467.1:n.510+42_510+52del
NM_005502.3:c.2337+42_2337+52del NP_005493.2:n.2337+42_2337+52del
XM_005251773.1:c.2337+42_2337+52del XP_005251830.1:n.2337+42_2337+52del
XM_005251776.1:c.2157+42_2157+52del XP_005251833.1:n.2157+42_2157+52del
XM_011518339.1:c.2412+42_2412+52del XP_011516641.1:n.2412+42_2412+52del
XM_011518340.1:c.2412+42_2412+52del XP_011516642.1:n.2412+42_2412+52del
XM_011518341.1:c.2412+42_2412+52del XP_011516643.1:n.2412+42_2412+52del
XM_011518342.1:c.1974+42_1974+52del XP_011516644.1:n.1974+42_1974+52del
XM_011518343.1:c.2412+42_2412+52del XP_011516645.1:n.2412+42_2412+52del
XM_011518344.1:c.2412+42_2412+52del XP_011516646.1:n.2412+42_2412+52del
XM_005251773.3:c.2337+42_2337+52del XP_005251830.1:n.2337+42_2337+52del
XM_005251776.3:c.2157+42_2157+52del XP_005251833.1:n.2157+42_2157+52del
XM_011518339.3:c.2412+42_2412+52del XP_011516641.1:n.2412+42_2412+52del
XM_011518340.3:c.2412+42_2412+52del XP_011516642.1:n.2412+42_2412+52del
XM_011518341.3:c.2412+42_2412+52del XP_011516643.1:n.2412+42_2412+52del
XM_011518342.3:c.1974+42_1974+52del XP_011516644.1:n.1974+42_1974+52del
XM_011518344.2:c.2412+42_2412+52del XP_011516646.1:n.2412+42_2412+52del
XM_017014378.2:c.2412+42_2412+52del XP_016869867.1:n.2412+42_2412+52del
XM_017014379.2:c.2412+42_2412+52del XP_016869868.1:n.2412+42_2412+52del
XM_017014380.2:c.2412+42_2412+52del XP_016869869.1:n.2412+42_2412+52del
XM_017014381.2:c.2412+42_2412+52del XP_016869870.1:n.2412+42_2412+52del
XM_017014382.2:c.2274+42_2274+52del XP_016869871.1:n.2274+42_2274+52del
XR_001746223.1:n.2725+42_2725+52del
NM_005502.4:c.2337+42_2337+52del MANE Select NP_005493.2:n.2337+42_2337+52del