Canonical Allele Identifier: CA1306201731
Gene: ABCB11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.168927866_168927870delinsCAACA , CM000664.2:g.168927866_168927870delinsCAACA GRCh38
NC_000002.11:g.169784376_169784380delinsCAACA , CM000664.1:g.169784376_169784380delinsCAACA GRCh37
NC_000002.10:g.169492622_169492626delinsCAACA NCBI36
NG_007374.1:g.108454_108458delinsTGTTG
NG_007374.2:g.108527_108531delinsTGTTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000649448.1:c.1789-508_1789-504delinsTGTTG ENSP00000497165.1:n.1789-508_1789-504delinsTGTTG
ENST00000650372.1:c.3412-508_3412-504delinsTGTTG MANE Select ENSP00000497931.1:n.3412-508_3412-504delinsTGTTG
ENST00000263817.6:c.3412-508_3412-504delinsTGTTG ENSP00000263817.6:n.3412-508_3412-504delinsTGTTG
ENST00000439188.1:c.2101-580_2101-576delinsTGTTG ENSP00000416058.1:n.2101-580_2101-576delinsTGTTG
NM_003742.2:c.3412-508_3412-504delinsTGTTG NP_003733.2:n.3412-508_3412-504delinsTGTTG
XM_006712817.2:c.3454-508_3454-504delinsTGTTG XP_006712880.1:n.3454-508_3454-504delinsTGTTG
XM_011512077.1:c.3514-508_3514-504delinsTGTTG XP_011510379.1:n.3514-508_3514-504delinsTGTTG
XM_011512078.1:c.3514-508_3514-504delinsTGTTG XP_011510380.1:n.3514-508_3514-504delinsTGTTG
XM_011512079.1:c.3514-508_3514-504delinsTGTTG XP_011510381.1:n.3514-508_3514-504delinsTGTTG
XM_011512081.1:c.1738-508_1738-504delinsTGTTG XP_011510383.1:n.1738-508_1738-504delinsTGTTG
NM_003742.4:c.3412-508_3412-504delinsTGTTG MANE Select NP_003733.2:n.3412-508_3412-504delinsTGTTG
XM_006712817.3:c.3454-508_3454-504delinsTGTTG XP_006712880.1:n.3454-508_3454-504delinsTGTTG
XM_011512077.2:c.3514-508_3514-504delinsTGTTG XP_011510379.1:n.3514-508_3514-504delinsTGTTG
XM_011512078.2:c.3514-508_3514-504delinsTGTTG XP_011510380.1:n.3514-508_3514-504delinsTGTTG
XM_011512081.2:c.1738-508_1738-504delinsTGTTG XP_011510383.1:n.1738-508_1738-504delinsTGTTG
XM_017005165.1:c.3514-508_3514-504delinsTGTTG XP_016860654.1:n.3514-508_3514-504delinsTGTTG
XM_017005166.1:c.2743-508_2743-504delinsTGTTG XP_016860655.1:n.2743-508_2743-504delinsTGTTG
XM_017005167.1:c.2197-508_2197-504delinsTGTTG XP_016860656.1:n.2197-508_2197-504delinsTGTTG