Canonical Allele Identifier: CA1723631797

Gene: ABCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87530953_87530957delinsAGAAG , CM000669.2:g.87530953_87530957delinsAGAAG	GRCh38
NC_000007.13:g.87160269_87160273delinsAGAAG , CM000669.1:g.87160269_87160273delinsAGAAG	GRCh37
NC_000007.12:g.86998205_86998209delinsAGAAG	NCBI36
NG_011513.1:g.187292_187296delinsCTTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.2685+337_2685+341delinsCTTCT	ENSP00000265724.3:n.2685+337_2685+341delinsCTTCT
ENST00000622132.5:c.2685+337_2685+341delinsCTTCT MANE Select	ENSP00000478255.1:n.2685+337_2685+341delinsCTTCT
ENST00000265724.7:c.2685+337_2685+341delinsCTTCT	ENSP00000265724.3:n.2685+337_2685+341delinsCTTCT
ENST00000488737.6:n.327+337_327+341delinsCTTCT
ENST00000496821.5:n.313+337_313+341delinsCTTCT
ENST00000543898.5:c.2493+337_2493+341delinsCTTCT	ENSP00000444095.1:n.2493+337_2493+341delinsCTTCT
ENST00000622132.4:c.2685+337_2685+341delinsCTTCT	ENSP00000478255.1:n.2685+337_2685+341delinsCTTCT
NM_000927.4:c.2685+337_2685+341delinsCTTCT	NP_000918.2:n.2685+337_2685+341delinsCTTCT
NM_001348944.1:c.2685+337_2685+341delinsCTTCT	NP_001335873.1:n.2685+337_2685+341delinsCTTCT
NM_001348945.1:c.2895+337_2895+341delinsCTTCT	NP_001335874.1:n.2895+337_2895+341delinsCTTCT
NM_001348946.1:c.2685+337_2685+341delinsCTTCT	NP_001335875.1:n.2685+337_2685+341delinsCTTCT
NM_001348946.2:c.2685+337_2685+341delinsCTTCT MANE Select	NP_001335875.1:n.2685+337_2685+341delinsCTTCT
NM_000927.5:c.2685+337_2685+341delinsCTTCT	NP_000918.2:n.2685+337_2685+341delinsCTTCT
NM_001348944.2:c.2685+337_2685+341delinsCTTCT	NP_001335873.1:n.2685+337_2685+341delinsCTTCT
NM_001348945.2:c.2895+337_2895+341delinsCTTCT	NP_001335874.1:n.2895+337_2895+341delinsCTTCT