Canonical Allele Identifier: CA3041046896
Gene: ABCB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87530941_87530950del , CM000669.2:g.87530941_87530950del GRCh38
NC_000007.13:g.87160257_87160266del , CM000669.1:g.87160257_87160266del GRCh37
NC_000007.12:g.86998193_86998202del NCBI36
NG_011513.1:g.187299_187308del

Transcript Alleles

HGVS Amino-acid Change
ENST00000265724.8:c.2685+344_2685+353del ENSP00000265724.3:n.2685+344_2685+353del
ENST00000622132.5:c.2685+344_2685+353del MANE Select ENSP00000478255.1:n.2685+344_2685+353del
ENST00000265724.7:c.2685+344_2685+353del ENSP00000265724.3:n.2685+344_2685+353del
ENST00000488737.6:n.327+344_327+353del
ENST00000496821.5:n.313+344_313+353del
ENST00000543898.5:c.2493+344_2493+353del ENSP00000444095.1:n.2493+344_2493+353del
ENST00000622132.4:c.2685+344_2685+353del ENSP00000478255.1:n.2685+344_2685+353del
NM_000927.4:c.2685+344_2685+353del NP_000918.2:n.2685+344_2685+353del
NM_001348944.1:c.2685+344_2685+353del NP_001335873.1:n.2685+344_2685+353del
NM_001348945.1:c.2895+344_2895+353del NP_001335874.1:n.2895+344_2895+353del
NM_001348946.1:c.2685+344_2685+353del NP_001335875.1:n.2685+344_2685+353del
NM_001348946.2:c.2685+344_2685+353del MANE Select NP_001335875.1:n.2685+344_2685+353del
NM_000927.5:c.2685+344_2685+353del NP_000918.2:n.2685+344_2685+353del
NM_001348944.2:c.2685+344_2685+353del NP_001335873.1:n.2685+344_2685+353del
NM_001348945.2:c.2895+344_2895+353del NP_001335874.1:n.2895+344_2895+353del