Canonical Allele Identifier: CA1723630568

Gene: ABCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87530576_87530577delinsAG , CM000669.2:g.87530576_87530577delinsAG	GRCh38
NC_000007.13:g.87159892_87159893delinsAG , CM000669.1:g.87159892_87159893delinsAG	GRCh37
NC_000007.12:g.86997828_86997829delinsAG	NCBI36
NG_011513.1:g.187672_187673delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.2685+717_2685+718delinsCT	ENSP00000265724.3:n.2685+717_2685+718delinsCT
ENST00000622132.5:c.2685+717_2685+718delinsCT MANE Select	ENSP00000478255.1:n.2685+717_2685+718delinsCT
ENST00000265724.7:c.2685+717_2685+718delinsCT	ENSP00000265724.3:n.2685+717_2685+718delinsCT
ENST00000488737.6:n.327+717_327+718delinsCT
ENST00000496821.5:n.313+717_313+718delinsCT
ENST00000543898.5:c.2493+717_2493+718delinsCT	ENSP00000444095.1:n.2493+717_2493+718delinsCT
ENST00000622132.4:c.2685+717_2685+718delinsCT	ENSP00000478255.1:n.2685+717_2685+718delinsCT
NM_000927.4:c.2685+717_2685+718delinsCT	NP_000918.2:n.2685+717_2685+718delinsCT
NM_001348944.1:c.2685+717_2685+718delinsCT	NP_001335873.1:n.2685+717_2685+718delinsCT
NM_001348945.1:c.2895+717_2895+718delinsCT	NP_001335874.1:n.2895+717_2895+718delinsCT
NM_001348946.1:c.2685+717_2685+718delinsCT	NP_001335875.1:n.2685+717_2685+718delinsCT
NM_001348946.2:c.2685+717_2685+718delinsCT MANE Select	NP_001335875.1:n.2685+717_2685+718delinsCT
NM_000927.5:c.2685+717_2685+718delinsCT	NP_000918.2:n.2685+717_2685+718delinsCT
NM_001348944.2:c.2685+717_2685+718delinsCT	NP_001335873.1:n.2685+717_2685+718delinsCT
NM_001348945.2:c.2895+717_2895+718delinsCT	NP_001335874.1:n.2895+717_2895+718delinsCT