Canonical Allele Identifier: CA2577147905

Gene: ABCB11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.168924813dup , CM000664.2:g.168924813dup	GRCh38
NC_000002.11:g.169781323dup , CM000664.1:g.169781323dup	GRCh37
NC_000002.10:g.169489569dup	NCBI36
NG_007374.1:g.111517dup
NG_007374.2:g.111590dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648875.1:c.80-4dup
ENST00000649448.1:c.1996-4dup	ENSP00000497165.1:n.1996-4dup
ENST00000650372.1:c.3619-4dup MANE Select	ENSP00000497931.1:n.3619-4dup
ENST00000263817.6:c.3619-4dup	ENSP00000263817.6:n.3619-4dup
ENST00000439188.1:c.2236-4dup	ENSP00000416058.1:n.2236-4dup
NM_003742.2:c.3619-4dup	NP_003733.2:n.3619-4dup
XM_006712817.2:c.3661-4dup	XP_006712880.1:n.3661-4dup
XM_011512077.1:c.3721-4dup	XP_011510379.1:n.3721-4dup
XM_011512078.1:c.3721-4dup	XP_011510380.1:n.3721-4dup
XM_011512079.1:c.3721-4dup	XP_011510381.1:n.3721-4dup
XM_011512081.1:c.1945-4dup	XP_011510383.1:n.1945-4dup
NM_003742.4:c.3619-4dup MANE Select	NP_003733.2:n.3619-4dup
XM_006712817.3:c.3661-4dup	XP_006712880.1:n.3661-4dup
XM_011512077.2:c.3721-4dup	XP_011510379.1:n.3721-4dup
XM_011512078.2:c.3721-4dup	XP_011510380.1:n.3721-4dup
XM_011512081.2:c.1945-4dup	XP_011510383.1:n.1945-4dup
XM_017005165.1:c.3721-4dup	XP_016860654.1:n.3721-4dup
XM_017005166.1:c.2950-4dup	XP_016860655.1:n.2950-4dup
XM_017005167.1:c.2404-4dup	XP_016860656.1:n.2404-4dup