Canonical Allele Identifier: CA2776827699

Gene: ABCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87562920_87562921insTG , CM000669.2:g.87562920_87562921insTG	GRCh38
NC_000007.13:g.87192236_87192237insTG , CM000669.1:g.87192236_87192237insTG	GRCh37
NC_000007.12:g.87030172_87030173insTG	NCBI36
NG_011513.1:g.155329_155330insAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.703-1533_703-1532insAC	ENSP00000265724.3:n.703-1533_703-1532insAC
ENST00000622132.5:c.703-1533_703-1532insAC MANE Select	ENSP00000478255.1:n.703-1533_703-1532insAC
ENST00000265724.7:c.703-1533_703-1532insAC	ENSP00000265724.3:n.703-1533_703-1532insAC
ENST00000543898.5:c.511-1533_511-1532insAC	ENSP00000444095.1:n.511-1533_511-1532insAC
ENST00000622132.4:c.703-1533_703-1532insAC	ENSP00000478255.1:n.703-1533_703-1532insAC
NM_000927.4:c.703-1533_703-1532insAC	NP_000918.2:n.703-1533_703-1532insAC
NM_001348944.1:c.703-1533_703-1532insAC	NP_001335873.1:n.703-1533_703-1532insAC
NM_001348945.1:c.913-1533_913-1532insAC	NP_001335874.1:n.913-1533_913-1532insAC
NM_001348946.1:c.703-1533_703-1532insAC	NP_001335875.1:n.703-1533_703-1532insAC
NM_001348946.2:c.703-1533_703-1532insAC MANE Select	NP_001335875.1:n.703-1533_703-1532insAC
NM_000927.5:c.703-1533_703-1532insAC	NP_000918.2:n.703-1533_703-1532insAC
NM_001348944.2:c.703-1533_703-1532insAC	NP_001335873.1:n.703-1533_703-1532insAC
NM_001348945.2:c.913-1533_913-1532insAC	NP_001335874.1:n.913-1533_913-1532insAC