Canonical Allele Identifier: CA1723631095

Gene: ABCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87530818_87530825delinsAAAGCAAG , CM000669.2:g.87530818_87530825delinsAAAGCAAG	GRCh38
NC_000007.13:g.87160134_87160141delinsAAAGCAAG , CM000669.1:g.87160134_87160141delinsAAAGCAAG	GRCh37
NC_000007.12:g.86998070_86998077delinsAAAGCAAG	NCBI36
NG_011513.1:g.187424_187431delinsCTTGCTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.2685+469_2685+476delinsCTTGCTTT	ENSP00000265724.3:n.2685+469_2685+476delinsCTTGCTTT
ENST00000622132.5:c.2685+469_2685+476delinsCTTGCTTT MANE Select	ENSP00000478255.1:n.2685+469_2685+476delinsCTTGCTTT
ENST00000265724.7:c.2685+469_2685+476delinsCTTGCTTT	ENSP00000265724.3:n.2685+469_2685+476delinsCTTGCTTT
ENST00000488737.6:n.327+469_327+476delinsCTTGCTTT
ENST00000496821.5:n.313+469_313+476delinsCTTGCTTT
ENST00000543898.5:c.2493+469_2493+476delinsCTTGCTTT	ENSP00000444095.1:n.2493+469_2493+476delinsCTTGCTTT
ENST00000622132.4:c.2685+469_2685+476delinsCTTGCTTT	ENSP00000478255.1:n.2685+469_2685+476delinsCTTGCTTT
NM_000927.4:c.2685+469_2685+476delinsCTTGCTTT	NP_000918.2:n.2685+469_2685+476delinsCTTGCTTT
NM_001348944.1:c.2685+469_2685+476delinsCTTGCTTT	NP_001335873.1:n.2685+469_2685+476delinsCTTGCTTT
NM_001348945.1:c.2895+469_2895+476delinsCTTGCTTT	NP_001335874.1:n.2895+469_2895+476delinsCTTGCTTT
NM_001348946.1:c.2685+469_2685+476delinsCTTGCTTT	NP_001335875.1:n.2685+469_2685+476delinsCTTGCTTT
NM_001348946.2:c.2685+469_2685+476delinsCTTGCTTT MANE Select	NP_001335875.1:n.2685+469_2685+476delinsCTTGCTTT
NM_000927.5:c.2685+469_2685+476delinsCTTGCTTT	NP_000918.2:n.2685+469_2685+476delinsCTTGCTTT
NM_001348944.2:c.2685+469_2685+476delinsCTTGCTTT	NP_001335873.1:n.2685+469_2685+476delinsCTTGCTTT
NM_001348945.2:c.2895+469_2895+476delinsCTTGCTTT	NP_001335874.1:n.2895+469_2895+476delinsCTTGCTTT