Canonical Allele Identifier: CA1723645220
Gene: ABCB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87562884_87562893delinsAGGCCAAGAG , CM000669.2:g.87562884_87562893delinsAGGCCAAGAG GRCh38
NC_000007.13:g.87192200_87192209delinsAGGCCAAGAG , CM000669.1:g.87192200_87192209delinsAGGCCAAGAG GRCh37
NC_000007.12:g.87030136_87030145delinsAGGCCAAGAG NCBI36
NG_011513.1:g.155356_155365delinsCTCTTGGCCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000265724.8:c.703-1506_703-1497delinsCTCTTGGCCT ENSP00000265724.3:n.703-1506_703-1497delinsCTCTTGGCCT
ENST00000622132.5:c.703-1506_703-1497delinsCTCTTGGCCT MANE Select ENSP00000478255.1:n.703-1506_703-1497delinsCTCTTGGCCT
ENST00000265724.7:c.703-1506_703-1497delinsCTCTTGGCCT ENSP00000265724.3:n.703-1506_703-1497delinsCTCTTGGCCT
ENST00000543898.5:c.511-1506_511-1497delinsCTCTTGGCCT ENSP00000444095.1:n.511-1506_511-1497delinsCTCTTGGCCT
ENST00000622132.4:c.703-1506_703-1497delinsCTCTTGGCCT ENSP00000478255.1:n.703-1506_703-1497delinsCTCTTGGCCT
NM_000927.4:c.703-1506_703-1497delinsCTCTTGGCCT NP_000918.2:n.703-1506_703-1497delinsCTCTTGGCCT
NM_001348944.1:c.703-1506_703-1497delinsCTCTTGGCCT NP_001335873.1:n.703-1506_703-1497delinsCTCTTGGCCT
NM_001348945.1:c.913-1506_913-1497delinsCTCTTGGCCT NP_001335874.1:n.913-1506_913-1497delinsCTCTTGGCCT
NM_001348946.1:c.703-1506_703-1497delinsCTCTTGGCCT NP_001335875.1:n.703-1506_703-1497delinsCTCTTGGCCT
NM_001348946.2:c.703-1506_703-1497delinsCTCTTGGCCT MANE Select NP_001335875.1:n.703-1506_703-1497delinsCTCTTGGCCT
NM_000927.5:c.703-1506_703-1497delinsCTCTTGGCCT NP_000918.2:n.703-1506_703-1497delinsCTCTTGGCCT
NM_001348944.2:c.703-1506_703-1497delinsCTCTTGGCCT NP_001335873.1:n.703-1506_703-1497delinsCTCTTGGCCT
NM_001348945.2:c.913-1506_913-1497delinsCTCTTGGCCT NP_001335874.1:n.913-1506_913-1497delinsCTCTTGGCCT