Canonical Allele Identifier: CA2683605480
Gene: ABCB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87516800_87516801insTG , CM000669.2:g.87516800_87516801insTG GRCh38
NC_000007.13:g.87146116_87146117insTG , CM000669.1:g.87146116_87146117insTG GRCh37
NC_000007.12:g.86984052_86984053insTG NCBI36
NG_011513.1:g.201448_201449insCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000265724.8:c.2928-136_2928-135insCA ENSP00000265724.3:n.2928-136_2928-135insCA
ENST00000622132.5:c.2928-136_2928-135insCA MANE Select ENSP00000478255.1:n.2928-136_2928-135insCA
ENST00000265724.7:c.2928-136_2928-135insCA ENSP00000265724.3:n.2928-136_2928-135insCA
ENST00000475929.5:n.84-136_84-135insCA
ENST00000483831.1:n.486-136_486-135insCA
ENST00000488737.6:n.570-136_570-135insCA
ENST00000496821.5:n.556-136_556-135insCA
ENST00000543898.5:c.2736-136_2736-135insCA ENSP00000444095.1:n.2736-136_2736-135insCA
ENST00000622132.4:c.2928-136_2928-135insCA ENSP00000478255.1:n.2928-136_2928-135insCA
NM_000927.4:c.2928-136_2928-135insCA NP_000918.2:n.2928-136_2928-135insCA
NM_001348944.1:c.2928-136_2928-135insCA NP_001335873.1:n.2928-136_2928-135insCA
NM_001348945.1:c.3138-136_3138-135insCA NP_001335874.1:n.3138-136_3138-135insCA
NM_001348946.1:c.2928-136_2928-135insCA NP_001335875.1:n.2928-136_2928-135insCA
NM_001348946.2:c.2928-136_2928-135insCA MANE Select NP_001335875.1:n.2928-136_2928-135insCA
NM_000927.5:c.2928-136_2928-135insCA NP_000918.2:n.2928-136_2928-135insCA
NM_001348944.2:c.2928-136_2928-135insCA NP_001335873.1:n.2928-136_2928-135insCA
NM_001348945.2:c.3138-136_3138-135insCA NP_001335874.1:n.3138-136_3138-135insCA