Canonical Allele Identifier: CA1306213449
Gene: ABCB11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.168944579_168944580delinsCT , CM000664.2:g.168944579_168944580delinsCT GRCh38
NC_000002.11:g.169801089_169801090delinsCT , CM000664.1:g.169801089_169801090delinsCT GRCh37
NC_000002.10:g.169509335_169509336delinsCT NCBI36
NG_007374.1:g.91744_91745delinsAG
NG_007374.2:g.91817_91818delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000649448.1:c.927+25_927+26delinsAG ENSP00000497165.1:n.927+25_927+26delinsAG
ENST00000650372.1:c.2610+25_2610+26delinsAG MANE Select ENSP00000497931.1:n.2610+25_2610+26delinsAG
ENST00000263817.6:c.2610+25_2610+26delinsAG ENSP00000263817.6:n.2610+25_2610+26delinsAG
ENST00000439188.1:c.1299+25_1299+26delinsAG ENSP00000416058.1:n.1299+25_1299+26delinsAG
NM_003742.2:c.2610+25_2610+26delinsAG NP_003733.2:n.2610+25_2610+26delinsAG
XM_006712817.2:c.2652+25_2652+26delinsAG XP_006712880.1:n.2652+25_2652+26delinsAG
XM_011512077.1:c.2712+25_2712+26delinsAG XP_011510379.1:n.2712+25_2712+26delinsAG
XM_011512078.1:c.2712+25_2712+26delinsAG XP_011510380.1:n.2712+25_2712+26delinsAG
XM_011512079.1:c.2712+25_2712+26delinsAG XP_011510381.1:n.2712+25_2712+26delinsAG
XM_011512080.1:c.2712+25_2712+26delinsAG XP_011510382.1:n.2712+25_2712+26delinsAG
XM_011512081.1:c.936+25_936+26delinsAG XP_011510383.1:n.936+25_936+26delinsAG
NM_003742.4:c.2610+25_2610+26delinsAG MANE Select NP_003733.2:n.2610+25_2610+26delinsAG
XM_006712817.3:c.2652+25_2652+26delinsAG XP_006712880.1:n.2652+25_2652+26delinsAG
XM_011512077.2:c.2712+25_2712+26delinsAG XP_011510379.1:n.2712+25_2712+26delinsAG
XM_011512078.2:c.2712+25_2712+26delinsAG XP_011510380.1:n.2712+25_2712+26delinsAG
XM_011512080.2:c.2712+25_2712+26delinsAG XP_011510382.1:n.2712+25_2712+26delinsAG
XM_011512081.2:c.936+25_936+26delinsAG XP_011510383.1:n.936+25_936+26delinsAG
XM_017005165.1:c.2712+25_2712+26delinsAG XP_016860654.1:n.2712+25_2712+26delinsAG
XM_017005166.1:c.1941+25_1941+26delinsAG XP_016860655.1:n.1941+25_1941+26delinsAG
XM_017005167.1:c.1395+25_1395+26delinsAG XP_016860656.1:n.1395+25_1395+26delinsAG