Canonical Allele Identifier: CA1723639673
Gene: ABCB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87540201_87540202delinsAG , CM000669.2:g.87540201_87540202delinsAG GRCh38
NC_000007.13:g.87169517_87169518delinsAG , CM000669.1:g.87169517_87169518delinsAG GRCh37
NC_000007.12:g.87007453_87007454delinsAG NCBI36
NG_011513.1:g.178047_178048delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000265724.8:c.2320-857_2320-856delinsCT ENSP00000265724.3:n.2320-857_2320-856delinsCT
ENST00000622132.5:c.2320-857_2320-856delinsCT MANE Select ENSP00000478255.1:n.2320-857_2320-856delinsCT
ENST00000265724.7:c.2320-857_2320-856delinsCT ENSP00000265724.3:n.2320-857_2320-856delinsCT
ENST00000543898.5:c.2128-857_2128-856delinsCT ENSP00000444095.1:n.2128-857_2128-856delinsCT
ENST00000622132.4:c.2320-857_2320-856delinsCT ENSP00000478255.1:n.2320-857_2320-856delinsCT
NM_000927.4:c.2320-857_2320-856delinsCT NP_000918.2:n.2320-857_2320-856delinsCT
NM_001348944.1:c.2320-857_2320-856delinsCT NP_001335873.1:n.2320-857_2320-856delinsCT
NM_001348945.1:c.2530-857_2530-856delinsCT NP_001335874.1:n.2530-857_2530-856delinsCT
NM_001348946.1:c.2320-857_2320-856delinsCT NP_001335875.1:n.2320-857_2320-856delinsCT
NM_001348946.2:c.2320-857_2320-856delinsCT MANE Select NP_001335875.1:n.2320-857_2320-856delinsCT
NM_000927.5:c.2320-857_2320-856delinsCT NP_000918.2:n.2320-857_2320-856delinsCT
NM_001348944.2:c.2320-857_2320-856delinsCT NP_001335873.1:n.2320-857_2320-856delinsCT
NM_001348945.2:c.2530-857_2530-856delinsCT NP_001335874.1:n.2530-857_2530-856delinsCT