Canonical Allele Identifier: CA1723631825
Gene: ABCB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87530970_87530972delinsGGA , CM000669.2:g.87530970_87530972delinsGGA GRCh38
NC_000007.13:g.87160286_87160288delinsGGA , CM000669.1:g.87160286_87160288delinsGGA GRCh37
NC_000007.12:g.86998222_86998224delinsGGA NCBI36
NG_011513.1:g.187277_187279delinsTCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000265724.8:c.2685+322_2685+324delinsTCC ENSP00000265724.3:n.2685+322_2685+324delinsTCC
ENST00000622132.5:c.2685+322_2685+324delinsTCC MANE Select ENSP00000478255.1:n.2685+322_2685+324delinsTCC
ENST00000265724.7:c.2685+322_2685+324delinsTCC ENSP00000265724.3:n.2685+322_2685+324delinsTCC
ENST00000488737.6:n.327+322_327+324delinsTCC
ENST00000496821.5:n.313+322_313+324delinsTCC
ENST00000543898.5:c.2493+322_2493+324delinsTCC ENSP00000444095.1:n.2493+322_2493+324delinsTCC
ENST00000622132.4:c.2685+322_2685+324delinsTCC ENSP00000478255.1:n.2685+322_2685+324delinsTCC
NM_000927.4:c.2685+322_2685+324delinsTCC NP_000918.2:n.2685+322_2685+324delinsTCC
NM_001348944.1:c.2685+322_2685+324delinsTCC NP_001335873.1:n.2685+322_2685+324delinsTCC
NM_001348945.1:c.2895+322_2895+324delinsTCC NP_001335874.1:n.2895+322_2895+324delinsTCC
NM_001348946.1:c.2685+322_2685+324delinsTCC NP_001335875.1:n.2685+322_2685+324delinsTCC
NM_001348946.2:c.2685+322_2685+324delinsTCC MANE Select NP_001335875.1:n.2685+322_2685+324delinsTCC
NM_000927.5:c.2685+322_2685+324delinsTCC NP_000918.2:n.2685+322_2685+324delinsTCC
NM_001348944.2:c.2685+322_2685+324delinsTCC NP_001335873.1:n.2685+322_2685+324delinsTCC
NM_001348945.2:c.2895+322_2895+324delinsTCC NP_001335874.1:n.2895+322_2895+324delinsTCC