Canonical Allele Identifier: CA162110804
Gene: ABCB1 HGNC NCBI

Linked Data

dbSNP Id: rs879169973

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87531265_87531269del , CM000669.2:g.87531265_87531269del GRCh38
NC_000007.13:g.87160581_87160585del , CM000669.1:g.87160581_87160585del GRCh37
NC_000007.12:g.86998517_86998521del NCBI36
NG_011513.1:g.186981_186985del

Transcript Alleles

HGVS Amino-acid change
ENST00000265724.8:c.2685+26_2685+30del ENSP00000265724.3:n.2685+26_2685+30del
ENST00000622132.5:c.2685+26_2685+30del MANE Select ENSP00000478255.1:n.2685+26_2685+30del
ENST00000265724.7:c.2685+26_2685+30del ENSP00000265724.3:n.2685+26_2685+30del
ENST00000488737.6:n.327+26_327+30del
ENST00000496821.5:n.313+26_313+30del
ENST00000543898.5:c.2493+26_2493+30del ENSP00000444095.1:n.2493+26_2493+30del
ENST00000622132.4:c.2685+26_2685+30del ENSP00000478255.1:n.2685+26_2685+30del
NM_000927.4:c.2685+26_2685+30del NP_000918.2:n.2685+26_2685+30del
NM_001348944.1:c.2685+26_2685+30del NP_001335873.1:n.2685+26_2685+30del
NM_001348945.1:c.2895+26_2895+30del NP_001335874.1:n.2895+26_2895+30del
NM_001348946.1:c.2685+26_2685+30del NP_001335875.1:n.2685+26_2685+30del
NM_001348946.2:c.2685+26_2685+30del MANE Select NP_001335875.1:n.2685+26_2685+30del
NM_000927.5:c.2685+26_2685+30del NP_000918.2:n.2685+26_2685+30del
NM_001348944.2:c.2685+26_2685+30del NP_001335873.1:n.2685+26_2685+30del
NM_001348945.2:c.2895+26_2895+30del NP_001335874.1:n.2895+26_2895+30del