Canonical Allele Identifier: CA2661805091
Gene: ABCB11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.168944678del , CM000664.2:g.168944678del GRCh38
NC_000002.11:g.169801188del , CM000664.1:g.169801188del GRCh37
NC_000002.10:g.169509434del NCBI36
NG_007374.1:g.91647del
NG_007374.2:g.91720del

Transcript Alleles

HGVS Amino-acid Change
ENST00000649448.1:c.855del ENSP00000497165.1:p.Trp285CysfsTer12
ENST00000650372.1:c.2538del MANE Select ENSP00000497931.1:p.Trp846CysfsTer12
ENST00000263817.6:c.2538del ENSP00000263817.6:p.Trp846CysfsTer12
ENST00000439188.1:c.1227del ENSP00000416058.1:n.1227del
NM_003742.2:c.2538del NP_003733.2:p.Trp846CysfsTer12
XM_006712817.2:c.2580del XP_006712880.1:p.Trp860CysfsTer12
XM_011512077.1:c.2640del XP_011510379.1:p.Trp880CysfsTer12
XM_011512078.1:c.2640del XP_011510380.1:p.Trp880CysfsTer12
XM_011512079.1:c.2640del XP_011510381.1:p.Trp880CysfsTer12
XM_011512080.1:c.2640del XP_011510382.1:p.Trp880CysfsTer12
XM_011512081.1:c.864del XP_011510383.1:p.Trp288CysfsTer12
NM_003742.4:c.2538del MANE Select NP_003733.2:p.Trp846CysfsTer12
XM_006712817.3:c.2580del XP_006712880.1:p.Trp860CysfsTer12
XM_011512077.2:c.2640del XP_011510379.1:p.Trp880CysfsTer12
XM_011512078.2:c.2640del XP_011510380.1:p.Trp880CysfsTer12
XM_011512080.2:c.2640del XP_011510382.1:p.Trp880CysfsTer12
XM_011512081.2:c.864del XP_011510383.1:p.Trp288CysfsTer12
XM_017005165.1:c.2640del XP_016860654.1:p.Trp880CysfsTer12
XM_017005166.1:c.1869del XP_016860655.1:p.Trp623CysfsTer12
XM_017005167.1:c.1323del XP_016860656.1:p.Trp441CysfsTer12