Canonical Allele Identifier: CA1723646413

Gene: ABCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87544846_87544848delinsTTC , CM000669.2:g.87544846_87544848delinsTTC	GRCh38
NC_000007.13:g.87174162_87174164delinsTTC , CM000669.1:g.87174162_87174164delinsTTC	GRCh37
NC_000007.12:g.87012098_87012100delinsTTC	NCBI36
NG_011513.1:g.173401_173403delinsGAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.2039_2041delinsGAA	ENSP00000265724.3:p.Arg680=
ENST00000622132.5:c.2039_2041delinsGAA MANE Select	ENSP00000478255.1:p.Arg680=
ENST00000265724.7:c.2039_2041delinsGAA	ENSP00000265724.3:p.Arg680=
ENST00000543898.5:c.1847_1849delinsGAA	ENSP00000444095.1:p.Arg616=
ENST00000622132.4:c.2039_2041delinsGAA	ENSP00000478255.1:p.Arg680=
NM_000927.4:c.2039_2041delinsGAA	NP_000918.2:p.Arg680=
NM_001348944.1:c.2039_2041delinsGAA	NP_001335873.1:p.Arg680=
NM_001348945.1:c.2249_2251delinsGAA	NP_001335874.1:p.Arg750=
NM_001348946.1:c.2039_2041delinsGAA	NP_001335875.1:p.Arg680=
NM_001348946.2:c.2039_2041delinsGAA MANE Select	NP_001335875.1:p.Arg680=
NM_000927.5:c.2039_2041delinsGAA	NP_000918.2:p.Arg680=
NM_001348944.2:c.2039_2041delinsGAA	NP_001335873.1:p.Arg680=
NM_001348945.2:c.2249_2251delinsGAA	NP_001335874.1:p.Arg750=