Canonical Allele Identifier: CA1306207199

Gene: ABCB11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.168944723A= , CM000664.2:g.168944723A=	GRCh38
NC_000002.11:g.169801233A= , CM000664.1:g.169801233A=	GRCh37
NC_000002.10:g.169509479A=	NCBI36
NG_007374.1:g.91601T=
NG_007374.2:g.91674T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649448.1:c.809T=	ENSP00000497165.1:p.Leu270=
ENST00000650372.1:c.2492T= MANE Select	ENSP00000497931.1:p.Leu831=
ENST00000263817.6:c.2492T=	ENSP00000263817.6:p.Leu831=
ENST00000439188.1:c.1181T=	ENSP00000416058.1:n.1181T=
NM_003742.2:c.2492T=	NP_003733.2:p.Leu831=
XM_006712817.2:c.2534T=	XP_006712880.1:p.Leu845=
XM_011512077.1:c.2594T=	XP_011510379.1:p.Leu865=
XM_011512078.1:c.2594T=	XP_011510380.1:p.Leu865=
XM_011512079.1:c.2594T=	XP_011510381.1:p.Leu865=
XM_011512080.1:c.2594T=	XP_011510382.1:p.Leu865=
XM_011512081.1:c.818T=	XP_011510383.1:p.Leu273=
NM_003742.4:c.2492T= MANE Select	NP_003733.2:p.Leu831=
XM_006712817.3:c.2534T=	XP_006712880.1:p.Leu845=
XM_011512077.2:c.2594T=	XP_011510379.1:p.Leu865=
XM_011512078.2:c.2594T=	XP_011510380.1:p.Leu865=
XM_011512080.2:c.2594T=	XP_011510382.1:p.Leu865=
XM_011512081.2:c.818T=	XP_011510383.1:p.Leu273=
XM_017005165.1:c.2594T=	XP_016860654.1:p.Leu865=
XM_017005166.1:c.1823T=	XP_016860655.1:p.Leu608=
XM_017005167.1:c.1277T=	XP_016860656.1:p.Leu426=