Canonical Allele Identifier: CA2776825843

Gene: ABCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87530858_87530859insCAGAAAGAAAGA , CM000669.2:g.87530858_87530859insCAGAAAGAAAGA	GRCh38
NC_000007.13:g.87160174_87160175insCAGAAAGAAAGA , CM000669.1:g.87160174_87160175insCAGAAAGAAAGA	GRCh37
NC_000007.12:g.86998110_86998111insCAGAAAGAAAGA	NCBI36
NG_011513.1:g.187401_187402insGTCTTTCTTTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.2685+446_2685+447insGTCTTTCTTTCT	ENSP00000265724.3:n.2685+446_2685+447insGTCTTTCTTTCT
ENST00000622132.5:c.2685+446_2685+447insGTCTTTCTTTCT MANE Select	ENSP00000478255.1:n.2685+446_2685+447insGTCTTTCTTTCT
ENST00000265724.7:c.2685+446_2685+447insGTCTTTCTTTCT	ENSP00000265724.3:n.2685+446_2685+447insGTCTTTCTTTCT
ENST00000488737.6:n.327+446_327+447insGTCTTTCTTTCT
ENST00000496821.5:n.313+446_313+447insGTCTTTCTTTCT
ENST00000543898.5:c.2493+446_2493+447insGTCTTTCTTTCT	ENSP00000444095.1:n.2493+446_2493+447insGTCTTTCTTTCT
ENST00000622132.4:c.2685+446_2685+447insGTCTTTCTTTCT	ENSP00000478255.1:n.2685+446_2685+447insGTCTTTCTTTCT
NM_000927.4:c.2685+446_2685+447insGTCTTTCTTTCT	NP_000918.2:n.2685+446_2685+447insGTCTTTCTTTCT
NM_001348944.1:c.2685+446_2685+447insGTCTTTCTTTCT	NP_001335873.1:n.2685+446_2685+447insGTCTTTCTTTCT
NM_001348945.1:c.2895+446_2895+447insGTCTTTCTTTCT	NP_001335874.1:n.2895+446_2895+447insGTCTTTCTTTCT
NM_001348946.1:c.2685+446_2685+447insGTCTTTCTTTCT	NP_001335875.1:n.2685+446_2685+447insGTCTTTCTTTCT
NM_001348946.2:c.2685+446_2685+447insGTCTTTCTTTCT MANE Select	NP_001335875.1:n.2685+446_2685+447insGTCTTTCTTTCT
NM_000927.5:c.2685+446_2685+447insGTCTTTCTTTCT	NP_000918.2:n.2685+446_2685+447insGTCTTTCTTTCT
NM_001348944.2:c.2685+446_2685+447insGTCTTTCTTTCT	NP_001335873.1:n.2685+446_2685+447insGTCTTTCTTTCT
NM_001348945.2:c.2895+446_2895+447insGTCTTTCTTTCT	NP_001335874.1:n.2895+446_2895+447insGTCTTTCTTTCT