Canonical Allele Identifier: CA1104126127
Gene: ABCB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87530851_87530860dup , CM000669.2:g.87530851_87530860dup GRCh38
NC_000007.13:g.87160167_87160176dup , CM000669.1:g.87160167_87160176dup GRCh37
NC_000007.12:g.86998103_86998112dup NCBI36
NG_011513.1:g.187390_187399dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000265724.8:c.2685+435_2685+444dup ENSP00000265724.3:n.2685+435_2685+444dup
ENST00000622132.5:c.2685+435_2685+444dup MANE Select ENSP00000478255.1:n.2685+435_2685+444dup
ENST00000265724.7:c.2685+435_2685+444dup ENSP00000265724.3:n.2685+435_2685+444dup
ENST00000488737.6:n.327+435_327+444dup
ENST00000496821.5:n.313+435_313+444dup
ENST00000543898.5:c.2493+435_2493+444dup ENSP00000444095.1:n.2493+435_2493+444dup
ENST00000622132.4:c.2685+435_2685+444dup ENSP00000478255.1:n.2685+435_2685+444dup
NM_000927.4:c.2685+435_2685+444dup NP_000918.2:n.2685+435_2685+444dup
NM_001348944.1:c.2685+435_2685+444dup NP_001335873.1:n.2685+435_2685+444dup
NM_001348945.1:c.2895+435_2895+444dup NP_001335874.1:n.2895+435_2895+444dup
NM_001348946.1:c.2685+435_2685+444dup NP_001335875.1:n.2685+435_2685+444dup
NM_001348946.2:c.2685+435_2685+444dup MANE Select NP_001335875.1:n.2685+435_2685+444dup
NM_000927.5:c.2685+435_2685+444dup NP_000918.2:n.2685+435_2685+444dup
NM_001348944.2:c.2685+435_2685+444dup NP_001335873.1:n.2685+435_2685+444dup
NM_001348945.2:c.2895+435_2895+444dup NP_001335874.1:n.2895+435_2895+444dup