Canonical Allele Identifier: CA1104126055
Gene: ABCB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87530841_87530842insCAAGAAAGAAAGAAAG , CM000669.2:g.87530841_87530842insCAAGAAAGAAAGAAAG GRCh38
NC_000007.13:g.87160157_87160158insCAAGAAAGAAAGAAAG , CM000669.1:g.87160157_87160158insCAAGAAAGAAAGAAAG GRCh37
NC_000007.12:g.86998093_86998094insCAAGAAAGAAAGAAAG NCBI36
NG_011513.1:g.187410_187411insTCTTTCTTTCTTGCTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000265724.8:c.2685+455_2685+456insTCTTTCTTTCTTGCTT ENSP00000265724.3:n.2685+455_2685+456insTCTTTCTTTCTTGCTT
ENST00000622132.5:c.2685+455_2685+456insTCTTTCTTTCTTGCTT MANE Select ENSP00000478255.1:n.2685+455_2685+456insTCTTTCTTTCTTGCTT
ENST00000265724.7:c.2685+455_2685+456insTCTTTCTTTCTTGCTT ENSP00000265724.3:n.2685+455_2685+456insTCTTTCTTTCTTGCTT
ENST00000488737.6:n.327+455_327+456insTCTTTCTTTCTTGCTT
ENST00000496821.5:n.313+455_313+456insTCTTTCTTTCTTGCTT
ENST00000543898.5:c.2493+455_2493+456insTCTTTCTTTCTTGCTT ENSP00000444095.1:n.2493+455_2493+456insTCTTTCTTTCTTGCTT
ENST00000622132.4:c.2685+455_2685+456insTCTTTCTTTCTTGCTT ENSP00000478255.1:n.2685+455_2685+456insTCTTTCTTTCTTGCTT
NM_000927.4:c.2685+455_2685+456insTCTTTCTTTCTTGCTT NP_000918.2:n.2685+455_2685+456insTCTTTCTTTCTTGCTT
NM_001348944.1:c.2685+455_2685+456insTCTTTCTTTCTTGCTT NP_001335873.1:n.2685+455_2685+456insTCTTTCTTTCTTGCTT
NM_001348945.1:c.2895+455_2895+456insTCTTTCTTTCTTGCTT NP_001335874.1:n.2895+455_2895+456insTCTTTCTTTCTTGCTT
NM_001348946.1:c.2685+455_2685+456insTCTTTCTTTCTTGCTT NP_001335875.1:n.2685+455_2685+456insTCTTTCTTTCTTGCTT
NM_001348946.2:c.2685+455_2685+456insTCTTTCTTTCTTGCTT MANE Select NP_001335875.1:n.2685+455_2685+456insTCTTTCTTTCTTGCTT
NM_000927.5:c.2685+455_2685+456insTCTTTCTTTCTTGCTT NP_000918.2:n.2685+455_2685+456insTCTTTCTTTCTTGCTT
NM_001348944.2:c.2685+455_2685+456insTCTTTCTTTCTTGCTT NP_001335873.1:n.2685+455_2685+456insTCTTTCTTTCTTGCTT
NM_001348945.2:c.2895+455_2895+456insTCTTTCTTTCTTGCTT NP_001335874.1:n.2895+455_2895+456insTCTTTCTTTCTTGCTT