Canonical Allele Identifier: CA1723630637

Gene: ABCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87530648_87530652delinsAAAAG , CM000669.2:g.87530648_87530652delinsAAAAG	GRCh38
NC_000007.13:g.87159964_87159968delinsAAAAG , CM000669.1:g.87159964_87159968delinsAAAAG	GRCh37
NC_000007.12:g.86997900_86997904delinsAAAAG	NCBI36
NG_011513.1:g.187597_187601delinsCTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.2685+642_2685+646delinsCTTTT	ENSP00000265724.3:n.2685+642_2685+646delinsCTTTT
ENST00000622132.5:c.2685+642_2685+646delinsCTTTT MANE Select	ENSP00000478255.1:n.2685+642_2685+646delinsCTTTT
ENST00000265724.7:c.2685+642_2685+646delinsCTTTT	ENSP00000265724.3:n.2685+642_2685+646delinsCTTTT
ENST00000488737.6:n.327+642_327+646delinsCTTTT
ENST00000496821.5:n.313+642_313+646delinsCTTTT
ENST00000543898.5:c.2493+642_2493+646delinsCTTTT	ENSP00000444095.1:n.2493+642_2493+646delinsCTTTT
ENST00000622132.4:c.2685+642_2685+646delinsCTTTT	ENSP00000478255.1:n.2685+642_2685+646delinsCTTTT
NM_000927.4:c.2685+642_2685+646delinsCTTTT	NP_000918.2:n.2685+642_2685+646delinsCTTTT
NM_001348944.1:c.2685+642_2685+646delinsCTTTT	NP_001335873.1:n.2685+642_2685+646delinsCTTTT
NM_001348945.1:c.2895+642_2895+646delinsCTTTT	NP_001335874.1:n.2895+642_2895+646delinsCTTTT
NM_001348946.1:c.2685+642_2685+646delinsCTTTT	NP_001335875.1:n.2685+642_2685+646delinsCTTTT
NM_001348946.2:c.2685+642_2685+646delinsCTTTT MANE Select	NP_001335875.1:n.2685+642_2685+646delinsCTTTT
NM_000927.5:c.2685+642_2685+646delinsCTTTT	NP_000918.2:n.2685+642_2685+646delinsCTTTT
NM_001348944.2:c.2685+642_2685+646delinsCTTTT	NP_001335873.1:n.2685+642_2685+646delinsCTTTT
NM_001348945.2:c.2895+642_2895+646delinsCTTTT	NP_001335874.1:n.2895+642_2895+646delinsCTTTT