Canonical Allele Identifier: CA1723621287

Gene: ABCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87503887_87503889delinsTAG , CM000669.2:g.87503887_87503889delinsTAG	GRCh38
NC_000007.13:g.87133203_87133205delinsTAG , CM000669.1:g.87133203_87133205delinsTAG	GRCh37
NC_000007.12:g.86971139_86971141delinsTAG	NCBI36
NG_011513.1:g.214360_214362delinsCTA

Transcript Alleles

HGVS	Amino-acid change
ENST00000265724.8:c.*354_*356delinsCTA	ENSP00000265724.3:n.*354_*356delinsCTA
ENST00000622132.5:c.*354_*356delinsCTA MANE Select	ENSP00000478255.1:n.*354_*356delinsCTA
ENST00000265724.7:c.*354_*356delinsCTA	ENSP00000265724.3:n.*354_*356delinsCTA
ENST00000488737.6:n.1839_1841delinsCTA
ENST00000543898.5:c.*354_*356delinsCTA	ENSP00000444095.1:n.*354_*356delinsCTA
ENST00000622132.4:c.*354_*356delinsCTA	ENSP00000478255.1:n.*354_*356delinsCTA
NM_000927.4:c.*354_*356delinsCTA	NP_000918.2:n.*354_*356delinsCTA
NM_001348944.1:c.*354_*356delinsCTA	NP_001335873.1:n.*354_*356delinsCTA
NM_001348945.1:c.*354_*356delinsCTA	NP_001335874.1:n.*354_*356delinsCTA
NM_001348946.1:c.*354_*356delinsCTA	NP_001335875.1:n.*354_*356delinsCTA
NM_001348946.2:c.*354_*356delinsCTA MANE Select	NP_001335875.1:n.*354_*356delinsCTA
NM_000927.5:c.*354_*356delinsCTA	NP_000918.2:n.*354_*356delinsCTA
NM_001348944.2:c.*354_*356delinsCTA	NP_001335873.1:n.*354_*356delinsCTA
NM_001348945.2:c.*354_*356delinsCTA	NP_001335874.1:n.*354_*356delinsCTA