Canonical Allele Identifier: CA429912433

Gene: ABCB11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.168923724G>A , CM000664.2:g.168923724G>A	GRCh38
NC_000002.11:g.169780234G>A , CM000664.1:g.169780234G>A	GRCh37
NC_000002.10:g.169488480G>A	NCBI36
NG_007374.1:g.112600C>T
NG_007374.2:g.112673C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648875.1:c.226+933C>T
ENST00000649448.1:c.2241C>T	ENSP00000497165.1:p.Val747=
ENST00000650372.1:c.3864C>T MANE Select	ENSP00000497931.1:p.Val1288=
ENST00000263817.6:c.3864C>T	ENSP00000263817.6:p.Val1288=
ENST00000439188.1:c.2481C>T	ENSP00000416058.1:n.2481C>T
NM_003742.2:c.3864C>T	NP_003733.2:p.Val1288=
XM_006712817.2:c.3906C>T	XP_006712880.1:p.Val1302=
XM_011512077.1:c.3966C>T	XP_011510379.1:p.Val1322=
XM_011512078.1:c.3966C>T	XP_011510380.1:p.Val1322=
XM_011512079.1:c.3966C>T	XP_011510381.1:p.Val1322=
XM_011512081.1:c.2190C>T	XP_011510383.1:p.Val730=
NM_003742.4:c.3864C>T MANE Select	NP_003733.2:p.Val1288=
XM_006712817.3:c.3906C>T	XP_006712880.1:p.Val1302=
XM_011512077.2:c.3966C>T	XP_011510379.1:p.Val1322=
XM_011512078.2:c.3966C>T	XP_011510380.1:p.Val1322=
XM_011512081.2:c.2190C>T	XP_011510383.1:p.Val730=
XM_017005165.1:c.3867+933C>T	XP_016860654.1:n.3867+933C>T
XM_017005166.1:c.3195C>T	XP_016860655.1:p.Val1065=
XM_017005167.1:c.2649C>T	XP_016860656.1:p.Val883=