Canonical Allele Identifier: CA1306207383

Gene: ABCB11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.168944902A= , CM000664.2:g.168944902A=	GRCh38
NC_000002.11:g.169801412A= , CM000664.1:g.169801412A=	GRCh37
NC_000002.10:g.169509658A=	NCBI36
NG_007374.1:g.91422T=
NG_007374.2:g.91495T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649448.1:c.720T=	ENSP00000497165.1:p.Leu240=
ENST00000650372.1:c.2403T= MANE Select	ENSP00000497931.1:p.Leu801=
ENST00000263817.6:c.2403T=	ENSP00000263817.6:p.Leu801=
ENST00000439188.1:c.1092T=	ENSP00000416058.1:n.1092T=
NM_003742.2:c.2403T=	NP_003733.2:p.Leu801=
XM_006712817.2:c.2445T=	XP_006712880.1:p.Leu815=
XM_011512077.1:c.2505T=	XP_011510379.1:p.Leu835=
XM_011512078.1:c.2505T=	XP_011510380.1:p.Leu835=
XM_011512079.1:c.2505T=	XP_011510381.1:p.Leu835=
XM_011512080.1:c.2505T=	XP_011510382.1:p.Leu835=
XM_011512081.1:c.729T=	XP_011510383.1:p.Leu243=
NM_003742.4:c.2403T= MANE Select	NP_003733.2:p.Leu801=
XM_006712817.3:c.2445T=	XP_006712880.1:p.Leu815=
XM_011512077.2:c.2505T=	XP_011510379.1:p.Leu835=
XM_011512078.2:c.2505T=	XP_011510380.1:p.Leu835=
XM_011512080.2:c.2505T=	XP_011510382.1:p.Leu835=
XM_011512081.2:c.729T=	XP_011510383.1:p.Leu243=
XM_017005165.1:c.2505T=	XP_016860654.1:p.Leu835=
XM_017005166.1:c.1734T=	XP_016860655.1:p.Leu578=
XM_017005167.1:c.1188T=	XP_016860656.1:p.Leu396=