Canonical Allele Identifier: CA1723645414

Gene: ABCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87563015_87563017delinsCAG , CM000669.2:g.87563015_87563017delinsCAG	GRCh38
NC_000007.13:g.87192331_87192333delinsCAG , CM000669.1:g.87192331_87192333delinsCAG	GRCh37
NC_000007.12:g.87030267_87030269delinsCAG	NCBI36
NG_011513.1:g.155232_155234delinsCTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000265724.8:c.703-1630_703-1628delinsCTG	ENSP00000265724.3:n.703-1630_703-1628delinsCTG
ENST00000622132.5:c.703-1630_703-1628delinsCTG MANE Select	ENSP00000478255.1:n.703-1630_703-1628delinsCTG
ENST00000265724.7:c.703-1630_703-1628delinsCTG	ENSP00000265724.3:n.703-1630_703-1628delinsCTG
ENST00000543898.5:c.511-1630_511-1628delinsCTG	ENSP00000444095.1:n.511-1630_511-1628delinsCTG
ENST00000622132.4:c.703-1630_703-1628delinsCTG	ENSP00000478255.1:n.703-1630_703-1628delinsCTG
NM_000927.4:c.703-1630_703-1628delinsCTG	NP_000918.2:n.703-1630_703-1628delinsCTG
NM_001348944.1:c.703-1630_703-1628delinsCTG	NP_001335873.1:n.703-1630_703-1628delinsCTG
NM_001348945.1:c.913-1630_913-1628delinsCTG	NP_001335874.1:n.913-1630_913-1628delinsCTG
NM_001348946.1:c.703-1630_703-1628delinsCTG	NP_001335875.1:n.703-1630_703-1628delinsCTG
NM_001348946.2:c.703-1630_703-1628delinsCTG MANE Select	NP_001335875.1:n.703-1630_703-1628delinsCTG
NM_000927.5:c.703-1630_703-1628delinsCTG	NP_000918.2:n.703-1630_703-1628delinsCTG
NM_001348944.2:c.703-1630_703-1628delinsCTG	NP_001335873.1:n.703-1630_703-1628delinsCTG
NM_001348945.2:c.913-1630_913-1628delinsCTG	NP_001335874.1:n.913-1630_913-1628delinsCTG