Canonical Allele Identifier: CA1723646927

Gene: ABCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87545199_87545202delinsAAAG , CM000669.2:g.87545199_87545202delinsAAAG	GRCh38
NC_000007.13:g.87174515_87174518delinsAAAG , CM000669.1:g.87174515_87174518delinsAAAG	GRCh37
NC_000007.12:g.87012451_87012454delinsAAAG	NCBI36
NG_011513.1:g.173047_173050delinsCTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.1888-203_1888-200delinsCTTT	ENSP00000265724.3:n.1888-203_1888-200delinsCTTT
ENST00000622132.5:c.1888-203_1888-200delinsCTTT MANE Select	ENSP00000478255.1:n.1888-203_1888-200delinsCTTT
ENST00000265724.7:c.1888-203_1888-200delinsCTTT	ENSP00000265724.3:n.1888-203_1888-200delinsCTTT
ENST00000543898.5:c.1696-203_1696-200delinsCTTT	ENSP00000444095.1:n.1696-203_1696-200delinsCTTT
ENST00000622132.4:c.1888-203_1888-200delinsCTTT	ENSP00000478255.1:n.1888-203_1888-200delinsCTTT
NM_000927.4:c.1888-203_1888-200delinsCTTT	NP_000918.2:n.1888-203_1888-200delinsCTTT
NM_001348944.1:c.1888-203_1888-200delinsCTTT	NP_001335873.1:n.1888-203_1888-200delinsCTTT
NM_001348945.1:c.2098-203_2098-200delinsCTTT	NP_001335874.1:n.2098-203_2098-200delinsCTTT
NM_001348946.1:c.1888-203_1888-200delinsCTTT	NP_001335875.1:n.1888-203_1888-200delinsCTTT
NM_001348946.2:c.1888-203_1888-200delinsCTTT MANE Select	NP_001335875.1:n.1888-203_1888-200delinsCTTT
NM_000927.5:c.1888-203_1888-200delinsCTTT	NP_000918.2:n.1888-203_1888-200delinsCTTT
NM_001348944.2:c.1888-203_1888-200delinsCTTT	NP_001335873.1:n.1888-203_1888-200delinsCTTT
NM_001348945.2:c.2098-203_2098-200delinsCTTT	NP_001335874.1:n.2098-203_2098-200delinsCTTT