Canonical Allele Identifier: CA1306213471

Gene: ABCB11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.168944621G= , CM000664.2:g.168944621G=	GRCh38
NC_000002.11:g.169801131G= , CM000664.1:g.169801131G=	GRCh37
NC_000002.10:g.169509377G=	NCBI36
NG_007374.1:g.91703C=
NG_007374.2:g.91776C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649448.1:c.911C=	ENSP00000497165.1:p.Ala304=
ENST00000650372.1:c.2594C= MANE Select	ENSP00000497931.1:p.Ala865=
ENST00000263817.6:c.2594C=	ENSP00000263817.6:p.Ala865=
ENST00000439188.1:c.1283C=	ENSP00000416058.1:n.1283C=
NM_003742.2:c.2594C=	NP_003733.2:p.Ala865=
XM_006712817.2:c.2636C=	XP_006712880.1:p.Ala879=
XM_011512077.1:c.2696C=	XP_011510379.1:p.Ala899=
XM_011512078.1:c.2696C=	XP_011510380.1:p.Ala899=
XM_011512079.1:c.2696C=	XP_011510381.1:p.Ala899=
XM_011512080.1:c.2696C=	XP_011510382.1:p.Ala899=
XM_011512081.1:c.920C=	XP_011510383.1:p.Ala307=
NM_003742.4:c.2594C= MANE Select	NP_003733.2:p.Ala865=
XM_006712817.3:c.2636C=	XP_006712880.1:p.Ala879=
XM_011512077.2:c.2696C=	XP_011510379.1:p.Ala899=
XM_011512078.2:c.2696C=	XP_011510380.1:p.Ala899=
XM_011512080.2:c.2696C=	XP_011510382.1:p.Ala899=
XM_011512081.2:c.920C=	XP_011510383.1:p.Ala307=
XM_017005165.1:c.2696C=	XP_016860654.1:p.Ala899=
XM_017005166.1:c.1925C=	XP_016860655.1:p.Ala642=
XM_017005167.1:c.1379C=	XP_016860656.1:p.Ala460=