Canonical Allele Identifier: CA1723661326

Gene: ABCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87599981_87599982delinsAT , CM000669.2:g.87599981_87599982delinsAT	GRCh38
NC_000007.13:g.87229297_87229298delinsAT , CM000669.1:g.87229297_87229298delinsAT	GRCh37
NC_000007.12:g.87067233_87067234delinsAT	NCBI36
NG_011513.1:g.118267_118268delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.68+135_68+136delinsAT	ENSP00000265724.3:n.68+135_68+136delinsAT
ENST00000622132.5:c.68+135_68+136delinsAT MANE Select	ENSP00000478255.1:n.68+135_68+136delinsAT
ENST00000265724.7:c.68+135_68+136delinsAT	ENSP00000265724.3:n.68+135_68+136delinsAT
ENST00000416177.1:c.68+135_68+136delinsAT	ENSP00000399419.1:n.68+135_68+136delinsAT
ENST00000543898.5:c.68+135_68+136delinsAT	ENSP00000444095.1:n.68+135_68+136delinsAT
ENST00000622132.4:c.68+135_68+136delinsAT	ENSP00000478255.1:n.68+135_68+136delinsAT
NM_000927.4:c.68+135_68+136delinsAT	NP_000918.2:n.68+135_68+136delinsAT
NM_001348944.1:c.68+135_68+136delinsAT	NP_001335873.1:n.68+135_68+136delinsAT
NM_001348945.1:c.278+135_278+136delinsAT	NP_001335874.1:n.278+135_278+136delinsAT
NM_001348946.1:c.68+135_68+136delinsAT	NP_001335875.1:n.68+135_68+136delinsAT
NM_001348946.2:c.68+135_68+136delinsAT MANE Select	NP_001335875.1:n.68+135_68+136delinsAT
NM_000927.5:c.68+135_68+136delinsAT	NP_000918.2:n.68+135_68+136delinsAT
NM_001348944.2:c.68+135_68+136delinsAT	NP_001335873.1:n.68+135_68+136delinsAT
NM_001348945.2:c.278+135_278+136delinsAT	NP_001335874.1:n.278+135_278+136delinsAT