Canonical Allele Identifier: CA1104126288
Gene: ABCB1 HGNC NCBI

Linked Data

dbSNP Id: rs1816029780

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87530953_87530956del , CM000669.2:g.87530953_87530956del GRCh38
NC_000007.13:g.87160269_87160272del , CM000669.1:g.87160269_87160272del GRCh37
NC_000007.12:g.86998205_86998208del NCBI36
NG_011513.1:g.187296_187299del

Transcript Alleles

HGVS Amino-acid Change
ENST00000265724.8:c.2685+341_2685+344del ENSP00000265724.3:n.2685+341_2685+344del
ENST00000622132.5:c.2685+341_2685+344del MANE Select ENSP00000478255.1:n.2685+341_2685+344del
ENST00000265724.7:c.2685+341_2685+344del ENSP00000265724.3:n.2685+341_2685+344del
ENST00000488737.6:n.327+341_327+344del
ENST00000496821.5:n.313+341_313+344del
ENST00000543898.5:c.2493+341_2493+344del ENSP00000444095.1:n.2493+341_2493+344del
ENST00000622132.4:c.2685+341_2685+344del ENSP00000478255.1:n.2685+341_2685+344del
NM_000927.4:c.2685+341_2685+344del NP_000918.2:n.2685+341_2685+344del
NM_001348944.1:c.2685+341_2685+344del NP_001335873.1:n.2685+341_2685+344del
NM_001348945.1:c.2895+341_2895+344del NP_001335874.1:n.2895+341_2895+344del
NM_001348946.1:c.2685+341_2685+344del NP_001335875.1:n.2685+341_2685+344del
NM_001348946.2:c.2685+341_2685+344del MANE Select NP_001335875.1:n.2685+341_2685+344del
NM_000927.5:c.2685+341_2685+344del NP_000918.2:n.2685+341_2685+344del
NM_001348944.2:c.2685+341_2685+344del NP_001335873.1:n.2685+341_2685+344del
NM_001348945.2:c.2895+341_2895+344del NP_001335874.1:n.2895+341_2895+344del