Canonical Allele Identifier: CA1723651731

Gene: ABCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87550365_87550366delinsAC , CM000669.2:g.87550365_87550366delinsAC	GRCh38
NC_000007.13:g.87179681_87179682delinsAC , CM000669.1:g.87179681_87179682delinsAC	GRCh37
NC_000007.12:g.87017617_87017618delinsAC	NCBI36
NG_011513.1:g.167883_167884delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.1225-70_1225-69delinsGT	ENSP00000265724.3:n.1225-70_1225-69delinsGT
ENST00000622132.5:c.1225-70_1225-69delinsGT MANE Select	ENSP00000478255.1:n.1225-70_1225-69delinsGT
ENST00000265724.7:c.1225-70_1225-69delinsGT	ENSP00000265724.3:n.1225-70_1225-69delinsGT
ENST00000543898.5:c.1033-70_1033-69delinsGT	ENSP00000444095.1:n.1033-70_1033-69delinsGT
ENST00000622132.4:c.1225-70_1225-69delinsGT	ENSP00000478255.1:n.1225-70_1225-69delinsGT
NM_000927.4:c.1225-70_1225-69delinsGT	NP_000918.2:n.1225-70_1225-69delinsGT
NM_001348944.1:c.1225-70_1225-69delinsGT	NP_001335873.1:n.1225-70_1225-69delinsGT
NM_001348945.1:c.1435-70_1435-69delinsGT	NP_001335874.1:n.1435-70_1435-69delinsGT
NM_001348946.1:c.1225-70_1225-69delinsGT	NP_001335875.1:n.1225-70_1225-69delinsGT
NM_001348946.2:c.1225-70_1225-69delinsGT MANE Select	NP_001335875.1:n.1225-70_1225-69delinsGT
NM_000927.5:c.1225-70_1225-69delinsGT	NP_000918.2:n.1225-70_1225-69delinsGT
NM_001348944.2:c.1225-70_1225-69delinsGT	NP_001335873.1:n.1225-70_1225-69delinsGT
NM_001348945.2:c.1435-70_1435-69delinsGT	NP_001335874.1:n.1435-70_1435-69delinsGT