Canonical Allele Identifier: CA1306201587

Gene: ABCB11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.168927665_168927666delinsCT , CM000664.2:g.168927665_168927666delinsCT	GRCh38
NC_000002.11:g.169784175_169784176delinsCT , CM000664.1:g.169784175_169784176delinsCT	GRCh37
NC_000002.10:g.169492421_169492422delinsCT	NCBI36
NG_007374.1:g.108658_108659delinsAG
NG_007374.2:g.108731_108732delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649448.1:c.1789-304_1789-303delinsAG	ENSP00000497165.1:n.1789-304_1789-303delinsAG
ENST00000650372.1:c.3412-304_3412-303delinsAG MANE Select	ENSP00000497931.1:n.3412-304_3412-303delinsAG
ENST00000263817.6:c.3412-304_3412-303delinsAG	ENSP00000263817.6:n.3412-304_3412-303delinsAG
ENST00000439188.1:c.2101-376_2101-375delinsAG	ENSP00000416058.1:n.2101-376_2101-375delinsAG
NM_003742.2:c.3412-304_3412-303delinsAG	NP_003733.2:n.3412-304_3412-303delinsAG
XM_006712817.2:c.3454-304_3454-303delinsAG	XP_006712880.1:n.3454-304_3454-303delinsAG
XM_011512077.1:c.3514-304_3514-303delinsAG	XP_011510379.1:n.3514-304_3514-303delinsAG
XM_011512078.1:c.3514-304_3514-303delinsAG	XP_011510380.1:n.3514-304_3514-303delinsAG
XM_011512079.1:c.3514-304_3514-303delinsAG	XP_011510381.1:n.3514-304_3514-303delinsAG
XM_011512081.1:c.1738-304_1738-303delinsAG	XP_011510383.1:n.1738-304_1738-303delinsAG
NM_003742.4:c.3412-304_3412-303delinsAG MANE Select	NP_003733.2:n.3412-304_3412-303delinsAG
XM_006712817.3:c.3454-304_3454-303delinsAG	XP_006712880.1:n.3454-304_3454-303delinsAG
XM_011512077.2:c.3514-304_3514-303delinsAG	XP_011510379.1:n.3514-304_3514-303delinsAG
XM_011512078.2:c.3514-304_3514-303delinsAG	XP_011510380.1:n.3514-304_3514-303delinsAG
XM_011512081.2:c.1738-304_1738-303delinsAG	XP_011510383.1:n.1738-304_1738-303delinsAG
XM_017005165.1:c.3514-304_3514-303delinsAG	XP_016860654.1:n.3514-304_3514-303delinsAG
XM_017005166.1:c.2743-304_2743-303delinsAG	XP_016860655.1:n.2743-304_2743-303delinsAG
XM_017005167.1:c.2197-304_2197-303delinsAG	XP_016860656.1:n.2197-304_2197-303delinsAG