Canonical Allele Identifier: CA645550358

Gene: ABCB1

Linked Data

• COSMIC: COSM4658186

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87516550_87516551insG , CM000669.2:g.87516550_87516551insG	GRCh38
NC_000007.13:g.87145866_87145867insG , CM000669.1:g.87145866_87145867insG	GRCh37
NC_000007.12:g.86983802_86983803insG	NCBI36
NG_011513.1:g.201698_201699insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.3042_3043insC	ENSP00000265724.3:p.Thr1015HisfsTer5
ENST00000622132.5:c.3042_3043insC MANE Select	ENSP00000478255.1:p.Thr1015HisfsTer5
ENST00000265724.7:c.3042_3043insC	ENSP00000265724.3:p.Thr1015HisfsTer5
ENST00000475929.5:n.198_199insC
ENST00000483831.1:n.600_601insC
ENST00000488737.6:n.684_685insC
ENST00000496821.5:n.670_671insC
ENST00000543898.5:c.2850_2851insC	ENSP00000444095.1:p.Thr951HisfsTer5
ENST00000622132.4:c.3042_3043insC	ENSP00000478255.1:p.Thr1015HisfsTer5
NM_000927.4:c.3042_3043insC	NP_000918.2:p.Thr1015HisfsTer5
NM_001348944.1:c.3042_3043insC	NP_001335873.1:p.Thr1015HisfsTer5
NM_001348945.1:c.3252_3253insC	NP_001335874.1:p.Thr1085HisfsTer5
NM_001348946.1:c.3042_3043insC	NP_001335875.1:p.Thr1015HisfsTer5
NM_001348946.2:c.3042_3043insC MANE Select	NP_001335875.1:p.Thr1015HisfsTer5
NM_000927.5:c.3042_3043insC	NP_000918.2:p.Thr1015HisfsTer5
NM_001348944.2:c.3042_3043insC	NP_001335873.1:p.Thr1015HisfsTer5
NM_001348945.2:c.3252_3253insC	NP_001335874.1:p.Thr1085HisfsTer5