Canonical Allele Identifier: CA1723658114
Gene: ABCB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87583724_87583729delinsCTTAGT , CM000669.2:g.87583724_87583729delinsCTTAGT GRCh38
NC_000007.13:g.87213040_87213045delinsCTTAGT , CM000669.1:g.87213040_87213045delinsCTTAGT GRCh37
NC_000007.12:g.87050976_87050981delinsCTTAGT NCBI36
NG_011513.1:g.134520_134525delinsACTAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000265724.8:c.286+1783_286+1788delinsACTAAG ENSP00000265724.3:n.286+1783_286+1788delinsACTAAG
ENST00000622132.5:c.286+1783_286+1788delinsACTAAG MANE Select ENSP00000478255.1:n.286+1783_286+1788delinsACTAAG
ENST00000265724.7:c.286+1783_286+1788delinsACTAAG ENSP00000265724.3:n.286+1783_286+1788delinsACTAAG
ENST00000543898.5:c.286+1783_286+1788delinsACTAAG ENSP00000444095.1:n.286+1783_286+1788delinsACTAAG
ENST00000622132.4:c.286+1783_286+1788delinsACTAAG ENSP00000478255.1:n.286+1783_286+1788delinsACTAAG
NM_000927.4:c.286+1783_286+1788delinsACTAAG NP_000918.2:n.286+1783_286+1788delinsACTAAG
NM_001348944.1:c.286+1783_286+1788delinsACTAAG NP_001335873.1:n.286+1783_286+1788delinsACTAAG
NM_001348945.1:c.496+1783_496+1788delinsACTAAG NP_001335874.1:n.496+1783_496+1788delinsACTAAG
NM_001348946.1:c.286+1783_286+1788delinsACTAAG NP_001335875.1:n.286+1783_286+1788delinsACTAAG
NM_001348946.2:c.286+1783_286+1788delinsACTAAG MANE Select NP_001335875.1:n.286+1783_286+1788delinsACTAAG
NM_000927.5:c.286+1783_286+1788delinsACTAAG NP_000918.2:n.286+1783_286+1788delinsACTAAG
NM_001348944.2:c.286+1783_286+1788delinsACTAAG NP_001335873.1:n.286+1783_286+1788delinsACTAAG
NM_001348945.2:c.496+1783_496+1788delinsACTAAG NP_001335874.1:n.496+1783_496+1788delinsACTAAG