Canonical Allele Identifier: CA1723646275
Gene: ABCB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87544756_87544760delinsCCTAG , CM000669.2:g.87544756_87544760delinsCCTAG GRCh38
NC_000007.13:g.87174072_87174076delinsCCTAG , CM000669.1:g.87174072_87174076delinsCCTAG GRCh37
NC_000007.12:g.87012008_87012012delinsCCTAG NCBI36
NG_011513.1:g.173489_173493delinsCTAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000265724.8:c.2064+63_2064+67delinsCTAGG ENSP00000265724.3:n.2064+63_2064+67delinsCTAGG
ENST00000622132.5:c.2064+63_2064+67delinsCTAGG MANE Select ENSP00000478255.1:n.2064+63_2064+67delinsCTAGG
ENST00000265724.7:c.2064+63_2064+67delinsCTAGG ENSP00000265724.3:n.2064+63_2064+67delinsCTAGG
ENST00000543898.5:c.1872+63_1872+67delinsCTAGG ENSP00000444095.1:n.1872+63_1872+67delinsCTAGG
ENST00000622132.4:c.2064+63_2064+67delinsCTAGG ENSP00000478255.1:n.2064+63_2064+67delinsCTAGG
NM_000927.4:c.2064+63_2064+67delinsCTAGG NP_000918.2:n.2064+63_2064+67delinsCTAGG
NM_001348944.1:c.2064+63_2064+67delinsCTAGG NP_001335873.1:n.2064+63_2064+67delinsCTAGG
NM_001348945.1:c.2274+63_2274+67delinsCTAGG NP_001335874.1:n.2274+63_2274+67delinsCTAGG
NM_001348946.1:c.2064+63_2064+67delinsCTAGG NP_001335875.1:n.2064+63_2064+67delinsCTAGG
NM_001348946.2:c.2064+63_2064+67delinsCTAGG MANE Select NP_001335875.1:n.2064+63_2064+67delinsCTAGG
NM_000927.5:c.2064+63_2064+67delinsCTAGG NP_000918.2:n.2064+63_2064+67delinsCTAGG
NM_001348944.2:c.2064+63_2064+67delinsCTAGG NP_001335873.1:n.2064+63_2064+67delinsCTAGG
NM_001348945.2:c.2274+63_2274+67delinsCTAGG NP_001335874.1:n.2274+63_2274+67delinsCTAGG