Canonical Allele Identifier: CA1306207365

Gene: ABCB11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.168944892T= , CM000664.2:g.168944892T=	GRCh38
NC_000002.11:g.169801402T= , CM000664.1:g.169801402T=	GRCh37
NC_000002.10:g.169509648T=	NCBI36
NG_007374.1:g.91432A=
NG_007374.2:g.91505A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649448.1:c.730A=	ENSP00000497165.1:p.Met244=
ENST00000650372.1:c.2413A= MANE Select	ENSP00000497931.1:p.Met805=
ENST00000263817.6:c.2413A=	ENSP00000263817.6:p.Met805=
ENST00000439188.1:c.1102A=	ENSP00000416058.1:n.1102A=
NM_003742.2:c.2413A=	NP_003733.2:p.Met805=
XM_006712817.2:c.2455A=	XP_006712880.1:p.Met819=
XM_011512077.1:c.2515A=	XP_011510379.1:p.Met839=
XM_011512078.1:c.2515A=	XP_011510380.1:p.Met839=
XM_011512079.1:c.2515A=	XP_011510381.1:p.Met839=
XM_011512080.1:c.2515A=	XP_011510382.1:p.Met839=
XM_011512081.1:c.739A=	XP_011510383.1:p.Met247=
NM_003742.4:c.2413A= MANE Select	NP_003733.2:p.Met805=
XM_006712817.3:c.2455A=	XP_006712880.1:p.Met819=
XM_011512077.2:c.2515A=	XP_011510379.1:p.Met839=
XM_011512078.2:c.2515A=	XP_011510380.1:p.Met839=
XM_011512080.2:c.2515A=	XP_011510382.1:p.Met839=
XM_011512081.2:c.739A=	XP_011510383.1:p.Met247=
XM_017005165.1:c.2515A=	XP_016860654.1:p.Met839=
XM_017005166.1:c.1744A=	XP_016860655.1:p.Met582=
XM_017005167.1:c.1198A=	XP_016860656.1:p.Met400=