Canonical Allele Identifier: CA1723631367
Gene: ABCB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87536377_87536378delinsAC , CM000669.2:g.87536377_87536378delinsAC GRCh38
NC_000007.13:g.87165693_87165694delinsAC , CM000669.1:g.87165693_87165694delinsAC GRCh37
NC_000007.12:g.87003629_87003630delinsAC NCBI36
NG_011513.1:g.181871_181872delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000265724.8:c.2481+80_2481+81delinsGT ENSP00000265724.3:n.2481+80_2481+81delinsGT
ENST00000622132.5:c.2481+80_2481+81delinsGT MANE Select ENSP00000478255.1:n.2481+80_2481+81delinsGT
ENST00000265724.7:c.2481+80_2481+81delinsGT ENSP00000265724.3:n.2481+80_2481+81delinsGT
ENST00000496821.5:n.109+80_109+81delinsGT
ENST00000543898.5:c.2289+80_2289+81delinsGT ENSP00000444095.1:n.2289+80_2289+81delinsGT
ENST00000622132.4:c.2481+80_2481+81delinsGT ENSP00000478255.1:n.2481+80_2481+81delinsGT
NM_000927.4:c.2481+80_2481+81delinsGT NP_000918.2:n.2481+80_2481+81delinsGT
NM_001348944.1:c.2481+80_2481+81delinsGT NP_001335873.1:n.2481+80_2481+81delinsGT
NM_001348945.1:c.2691+80_2691+81delinsGT NP_001335874.1:n.2691+80_2691+81delinsGT
NM_001348946.1:c.2481+80_2481+81delinsGT NP_001335875.1:n.2481+80_2481+81delinsGT
NM_001348946.2:c.2481+80_2481+81delinsGT MANE Select NP_001335875.1:n.2481+80_2481+81delinsGT
NM_000927.5:c.2481+80_2481+81delinsGT NP_000918.2:n.2481+80_2481+81delinsGT
NM_001348944.2:c.2481+80_2481+81delinsGT NP_001335873.1:n.2481+80_2481+81delinsGT
NM_001348945.2:c.2691+80_2691+81delinsGT NP_001335874.1:n.2691+80_2691+81delinsGT