Canonical Allele Identifier: CA1723630658
Gene: ABCB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87536079_87536080delinsTC , CM000669.2:g.87536079_87536080delinsTC GRCh38
NC_000007.13:g.87165395_87165396delinsTC , CM000669.1:g.87165395_87165396delinsTC GRCh37
NC_000007.12:g.87003331_87003332delinsTC NCBI36
NG_011513.1:g.182169_182170delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000265724.8:c.2481+378_2481+379delinsGA ENSP00000265724.3:n.2481+378_2481+379delinsGA
ENST00000622132.5:c.2481+378_2481+379delinsGA MANE Select ENSP00000478255.1:n.2481+378_2481+379delinsGA
ENST00000265724.7:c.2481+378_2481+379delinsGA ENSP00000265724.3:n.2481+378_2481+379delinsGA
ENST00000496821.5:n.109+378_109+379delinsGA
ENST00000543898.5:c.2289+378_2289+379delinsGA ENSP00000444095.1:n.2289+378_2289+379delinsGA
ENST00000622132.4:c.2481+378_2481+379delinsGA ENSP00000478255.1:n.2481+378_2481+379delinsGA
NM_000927.4:c.2481+378_2481+379delinsGA NP_000918.2:n.2481+378_2481+379delinsGA
NM_001348944.1:c.2481+378_2481+379delinsGA NP_001335873.1:n.2481+378_2481+379delinsGA
NM_001348945.1:c.2691+378_2691+379delinsGA NP_001335874.1:n.2691+378_2691+379delinsGA
NM_001348946.1:c.2481+378_2481+379delinsGA NP_001335875.1:n.2481+378_2481+379delinsGA
NM_001348946.2:c.2481+378_2481+379delinsGA MANE Select NP_001335875.1:n.2481+378_2481+379delinsGA
NM_000927.5:c.2481+378_2481+379delinsGA NP_000918.2:n.2481+378_2481+379delinsGA
NM_001348944.2:c.2481+378_2481+379delinsGA NP_001335873.1:n.2481+378_2481+379delinsGA
NM_001348945.2:c.2691+378_2691+379delinsGA NP_001335874.1:n.2691+378_2691+379delinsGA