Canonical Allele Identifier: CA1306205653

Gene: ABCB11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.168923321_168923322delinsTG , CM000664.2:g.168923321_168923322delinsTG	GRCh38
NC_000002.11:g.169779831_169779832delinsTG , CM000664.1:g.169779831_169779832delinsTG	GRCh37
NC_000002.10:g.169488077_169488078delinsTG	NCBI36
NG_007374.1:g.113002_113003delinsCA
NG_007374.2:g.113075_113076delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648875.1:c.226+1335_226+1336delinsCA
ENST00000649448.1:c.2643_2644delinsCA	ENSP00000497165.1:n.2643_2644delinsCA
ENST00000650372.1:c.*300_*301delinsCA MANE Select	ENSP00000497931.1:n.*300_*301delinsCA
ENST00000263817.6:c.*300_*301delinsCA	ENSP00000263817.6:n.*300_*301delinsCA
NM_003742.2:c.*300_*301delinsCA	NP_003733.2:n.*300_*301delinsCA
XM_006712817.2:c.*300_*301delinsCA	XP_006712880.1:n.*300_*301delinsCA
XM_011512077.1:c.*300_*301delinsCA	XP_011510379.1:n.*300_*301delinsCA
XM_011512078.1:c.*254_*255delinsCA	XP_011510380.1:n.*254_*255delinsCA
XM_011512079.1:c.*300_*301delinsCA	XP_011510381.1:n.*300_*301delinsCA
XM_011512081.1:c.*300_*301delinsCA	XP_011510383.1:n.*300_*301delinsCA
NM_003742.4:c.*300_*301delinsCA MANE Select	NP_003733.2:n.*300_*301delinsCA
XM_006712817.3:c.*300_*301delinsCA	XP_006712880.1:n.*300_*301delinsCA
XM_011512077.2:c.*300_*301delinsCA	XP_011510379.1:n.*300_*301delinsCA
XM_011512078.2:c.*254_*255delinsCA	XP_011510380.1:n.*254_*255delinsCA
XM_011512081.2:c.*300_*301delinsCA	XP_011510383.1:n.*300_*301delinsCA
XM_017005165.1:c.3867+1335_3867+1336delinsCA	XP_016860654.1:n.3867+1335_3867+1336delinsCA
XM_017005166.1:c.*300_*301delinsCA	XP_016860655.1:n.*300_*301delinsCA
XM_017005167.1:c.*300_*301delinsCA	XP_016860656.1:n.*300_*301delinsCA