Canonical Allele Identifier: CA1723632133
Gene: ABCB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87531220_87531221delinsAG , CM000669.2:g.87531220_87531221delinsAG GRCh38
NC_000007.13:g.87160536_87160537delinsAG , CM000669.1:g.87160536_87160537delinsAG GRCh37
NC_000007.12:g.86998472_86998473delinsAG NCBI36
NG_011513.1:g.187028_187029delinsCT

Transcript Alleles

HGVS Amino-acid change
ENST00000265724.8:c.2685+73_2685+74delinsCT ENSP00000265724.3:n.2685+73_2685+74delins...
ENST00000622132.5:c.2685+73_2685+74delinsCT MANE Select ENSP00000478255.1:n.2685+73_2685+74delins...
ENST00000265724.7:c.2685+73_2685+74delinsCT ENSP00000265724.3:n.2685+73_2685+74delins...
ENST00000488737.6:n.327+73_327+74delinsCT
ENST00000496821.5:n.313+73_313+74delinsCT
ENST00000543898.5:c.2493+73_2493+74delinsCT ENSP00000444095.1:n.2493+73_2493+74delins...
ENST00000622132.4:c.2685+73_2685+74delinsCT ENSP00000478255.1:n.2685+73_2685+74delins...
NM_000927.4:c.2685+73_2685+74delinsCT NP_000918.2:n.2685+73_2685+74delinsCT
NM_001348944.1:c.2685+73_2685+74delinsCT NP_001335873.1:n.2685+73_2685+74delinsCT
NM_001348945.1:c.2895+73_2895+74delinsCT NP_001335874.1:n.2895+73_2895+74delinsCT
NM_001348946.1:c.2685+73_2685+74delinsCT NP_001335875.1:n.2685+73_2685+74delinsCT
NM_001348946.2:c.2685+73_2685+74delinsCT MANE Select NP_001335875.1:n.2685+73_2685+74delinsCT
NM_000927.5:c.2685+73_2685+74delinsCT NP_000918.2:n.2685+73_2685+74delinsCT
NM_001348944.2:c.2685+73_2685+74delinsCT NP_001335873.1:n.2685+73_2685+74delinsCT
NM_001348945.2:c.2895+73_2895+74delinsCT NP_001335874.1:n.2895+73_2895+74delinsCT