Canonical Allele Identifier: CA2776826575
Gene: ABCB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87516682_87516683insCCCC , CM000669.2:g.87516682_87516683insCCCC GRCh38
NC_000007.13:g.87145998_87145999insCCCC , CM000669.1:g.87145998_87145999insCCCC GRCh37
NC_000007.12:g.86983934_86983935insCCCC NCBI36
NG_011513.1:g.201567_201568insGGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000265724.8:c.2928-17_2928-16insGGGG ENSP00000265724.3:n.2928-17_2928-16insGGGG
ENST00000622132.5:c.2928-17_2928-16insGGGG MANE Select ENSP00000478255.1:n.2928-17_2928-16insGGGG
ENST00000265724.7:c.2928-17_2928-16insGGGG ENSP00000265724.3:n.2928-17_2928-16insGGGG
ENST00000475929.5:n.84-17_84-16insGGGG
ENST00000483831.1:n.486-17_486-16insGGGG
ENST00000488737.6:n.570-17_570-16insGGGG
ENST00000496821.5:n.556-17_556-16insGGGG
ENST00000543898.5:c.2736-17_2736-16insGGGG ENSP00000444095.1:n.2736-17_2736-16insGGGG
ENST00000622132.4:c.2928-17_2928-16insGGGG ENSP00000478255.1:n.2928-17_2928-16insGGGG
NM_000927.4:c.2928-17_2928-16insGGGG NP_000918.2:n.2928-17_2928-16insGGGG
NM_001348944.1:c.2928-17_2928-16insGGGG NP_001335873.1:n.2928-17_2928-16insGGGG
NM_001348945.1:c.3138-17_3138-16insGGGG NP_001335874.1:n.3138-17_3138-16insGGGG
NM_001348946.1:c.2928-17_2928-16insGGGG NP_001335875.1:n.2928-17_2928-16insGGGG
NM_001348946.2:c.2928-17_2928-16insGGGG MANE Select NP_001335875.1:n.2928-17_2928-16insGGGG
NM_000927.5:c.2928-17_2928-16insGGGG NP_000918.2:n.2928-17_2928-16insGGGG
NM_001348944.2:c.2928-17_2928-16insGGGG NP_001335873.1:n.2928-17_2928-16insGGGG
NM_001348945.2:c.3138-17_3138-16insGGGG NP_001335874.1:n.3138-17_3138-16insGGGG