Canonical Allele Identifier: CA1723658136

Gene: ABCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87583769_87583770delinsAT , CM000669.2:g.87583769_87583770delinsAT	GRCh38
NC_000007.13:g.87213085_87213086delinsAT , CM000669.1:g.87213085_87213086delinsAT	GRCh37
NC_000007.12:g.87051021_87051022delinsAT	NCBI36
NG_011513.1:g.134479_134480delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.286+1742_286+1743delinsAT	ENSP00000265724.3:n.286+1742_286+1743delinsAT
ENST00000622132.5:c.286+1742_286+1743delinsAT MANE Select	ENSP00000478255.1:n.286+1742_286+1743delinsAT
ENST00000265724.7:c.286+1742_286+1743delinsAT	ENSP00000265724.3:n.286+1742_286+1743delinsAT
ENST00000543898.5:c.286+1742_286+1743delinsAT	ENSP00000444095.1:n.286+1742_286+1743delinsAT
ENST00000622132.4:c.286+1742_286+1743delinsAT	ENSP00000478255.1:n.286+1742_286+1743delinsAT
NM_000927.4:c.286+1742_286+1743delinsAT	NP_000918.2:n.286+1742_286+1743delinsAT
NM_001348944.1:c.286+1742_286+1743delinsAT	NP_001335873.1:n.286+1742_286+1743delinsAT
NM_001348945.1:c.496+1742_496+1743delinsAT	NP_001335874.1:n.496+1742_496+1743delinsAT
NM_001348946.1:c.286+1742_286+1743delinsAT	NP_001335875.1:n.286+1742_286+1743delinsAT
NM_001348946.2:c.286+1742_286+1743delinsAT MANE Select	NP_001335875.1:n.286+1742_286+1743delinsAT
NM_000927.5:c.286+1742_286+1743delinsAT	NP_000918.2:n.286+1742_286+1743delinsAT
NM_001348944.2:c.286+1742_286+1743delinsAT	NP_001335873.1:n.286+1742_286+1743delinsAT
NM_001348945.2:c.496+1742_496+1743delinsAT	NP_001335874.1:n.496+1742_496+1743delinsAT