Canonical Allele Identifier: CA651731702

Gene: ABCB1

Linked Data

• COSMIC: COSN15377497

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87503884_87503885insG , CM000669.2:g.87503884_87503885insG	GRCh38
NC_000007.13:g.87133200_87133201insG , CM000669.1:g.87133200_87133201insG	GRCh37
NC_000007.12:g.86971136_86971137insG	NCBI36
NG_011513.1:g.214364_214365insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.*358_*359insC	ENSP00000265724.3:n.*358_*359insC
ENST00000622132.5:c.*358_*359insC MANE Select	ENSP00000478255.1:n.*358_*359insC
ENST00000265724.7:c.*358_*359insC	ENSP00000265724.3:n.*358_*359insC
ENST00000488737.6:n.1843_1844insC
ENST00000543898.5:c.*358_*359insC	ENSP00000444095.1:n.*358_*359insC
ENST00000622132.4:c.*358_*359insC	ENSP00000478255.1:n.*358_*359insC
NM_000927.4:c.*358_*359insC	NP_000918.2:n.*358_*359insC
NM_001348944.1:c.*358_*359insC	NP_001335873.1:n.*358_*359insC
NM_001348945.1:c.*358_*359insC	NP_001335874.1:n.*358_*359insC
NM_001348946.1:c.*358_*359insC	NP_001335875.1:n.*358_*359insC
NM_001348946.2:c.*358_*359insC MANE Select	NP_001335875.1:n.*358_*359insC
NM_000927.5:c.*358_*359insC	NP_000918.2:n.*358_*359insC
NM_001348944.2:c.*358_*359insC	NP_001335873.1:n.*358_*359insC
NM_001348945.2:c.*358_*359insC	NP_001335874.1:n.*358_*359insC