Canonical Allele Identifier: CA1723661334
Gene: ABCB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87600019_87600022delinsAAAC , CM000669.2:g.87600019_87600022delinsAAAC GRCh38
NC_000007.13:g.87229335_87229338delinsAAAC , CM000669.1:g.87229335_87229338delinsAAAC GRCh37
NC_000007.12:g.87067271_87067274delinsAAAC NCBI36
NG_011513.1:g.118227_118230delinsGTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000265724.8:c.68+95_68+98delinsGTTT ENSP00000265724.3:n.68+95_68+98delinsGTTT
ENST00000622132.5:c.68+95_68+98delinsGTTT MANE Select ENSP00000478255.1:n.68+95_68+98delinsGTTT
ENST00000265724.7:c.68+95_68+98delinsGTTT ENSP00000265724.3:n.68+95_68+98delinsGTTT
ENST00000416177.1:c.68+95_68+98delinsGTTT ENSP00000399419.1:n.68+95_68+98delinsGTTT
ENST00000543898.5:c.68+95_68+98delinsGTTT ENSP00000444095.1:n.68+95_68+98delinsGTTT
ENST00000622132.4:c.68+95_68+98delinsGTTT ENSP00000478255.1:n.68+95_68+98delinsGTTT
NM_000927.4:c.68+95_68+98delinsGTTT NP_000918.2:n.68+95_68+98delinsGTTT
NM_001348944.1:c.68+95_68+98delinsGTTT NP_001335873.1:n.68+95_68+98delinsGTTT
NM_001348945.1:c.278+95_278+98delinsGTTT NP_001335874.1:n.278+95_278+98delinsGTTT
NM_001348946.1:c.68+95_68+98delinsGTTT NP_001335875.1:n.68+95_68+98delinsGTTT
NM_001348946.2:c.68+95_68+98delinsGTTT MANE Select NP_001335875.1:n.68+95_68+98delinsGTTT
NM_000927.5:c.68+95_68+98delinsGTTT NP_000918.2:n.68+95_68+98delinsGTTT
NM_001348944.2:c.68+95_68+98delinsGTTT NP_001335873.1:n.68+95_68+98delinsGTTT
NM_001348945.2:c.278+95_278+98delinsGTTT NP_001335874.1:n.278+95_278+98delinsGTTT