Canonical Allele Identifier: CA1306207209

Gene: ABCB11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.168944731_168944732delinsTG , CM000664.2:g.168944731_168944732delinsTG	GRCh38
NC_000002.11:g.169801241_169801242delinsTG , CM000664.1:g.169801241_169801242delinsTG	GRCh37
NC_000002.10:g.169509487_169509488delinsTG	NCBI36
NG_007374.1:g.91592_91593delinsCA
NG_007374.2:g.91665_91666delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649448.1:c.800_801delinsCA	ENSP00000497165.1:p.Thr267=
ENST00000650372.1:c.2483_2484delinsCA MANE Select	ENSP00000497931.1:p.Thr828=
ENST00000263817.6:c.2483_2484delinsCA	ENSP00000263817.6:p.Thr828=
ENST00000439188.1:c.1172_1173delinsCA	ENSP00000416058.1:n.1172_1173delinsCA
NM_003742.2:c.2483_2484delinsCA	NP_003733.2:p.Thr828=
XM_006712817.2:c.2525_2526delinsCA	XP_006712880.1:p.Thr842=
XM_011512077.1:c.2585_2586delinsCA	XP_011510379.1:p.Thr862=
XM_011512078.1:c.2585_2586delinsCA	XP_011510380.1:p.Thr862=
XM_011512079.1:c.2585_2586delinsCA	XP_011510381.1:p.Thr862=
XM_011512080.1:c.2585_2586delinsCA	XP_011510382.1:p.Thr862=
XM_011512081.1:c.809_810delinsCA	XP_011510383.1:p.Thr270=
NM_003742.4:c.2483_2484delinsCA MANE Select	NP_003733.2:p.Thr828=
XM_006712817.3:c.2525_2526delinsCA	XP_006712880.1:p.Thr842=
XM_011512077.2:c.2585_2586delinsCA	XP_011510379.1:p.Thr862=
XM_011512078.2:c.2585_2586delinsCA	XP_011510380.1:p.Thr862=
XM_011512080.2:c.2585_2586delinsCA	XP_011510382.1:p.Thr862=
XM_011512081.2:c.809_810delinsCA	XP_011510383.1:p.Thr270=
XM_017005165.1:c.2585_2586delinsCA	XP_016860654.1:p.Thr862=
XM_017005166.1:c.1814_1815delinsCA	XP_016860655.1:p.Thr605=
XM_017005167.1:c.1268_1269delinsCA	XP_016860656.1:p.Thr423=