Canonical Allele Identifier: CA2601259712
Gene: ABCB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87530859_87530872dup , CM000669.2:g.87530859_87530872dup GRCh38
NC_000007.13:g.87160175_87160188dup , CM000669.1:g.87160175_87160188dup GRCh37
NC_000007.12:g.86998111_86998124dup NCBI36
NG_011513.1:g.187378_187391dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000265724.8:c.2685+423_2685+436dup ENSP00000265724.3:n.2685+423_2685+436dup
ENST00000622132.5:c.2685+423_2685+436dup MANE Select ENSP00000478255.1:n.2685+423_2685+436dup
ENST00000265724.7:c.2685+423_2685+436dup ENSP00000265724.3:n.2685+423_2685+436dup
ENST00000488737.6:n.327+423_327+436dup
ENST00000496821.5:n.313+423_313+436dup
ENST00000543898.5:c.2493+423_2493+436dup ENSP00000444095.1:n.2493+423_2493+436dup
ENST00000622132.4:c.2685+423_2685+436dup ENSP00000478255.1:n.2685+423_2685+436dup
NM_000927.4:c.2685+423_2685+436dup NP_000918.2:n.2685+423_2685+436dup
NM_001348944.1:c.2685+423_2685+436dup NP_001335873.1:n.2685+423_2685+436dup
NM_001348945.1:c.2895+423_2895+436dup NP_001335874.1:n.2895+423_2895+436dup
NM_001348946.1:c.2685+423_2685+436dup NP_001335875.1:n.2685+423_2685+436dup
NM_001348946.2:c.2685+423_2685+436dup MANE Select NP_001335875.1:n.2685+423_2685+436dup
NM_000927.5:c.2685+423_2685+436dup NP_000918.2:n.2685+423_2685+436dup
NM_001348944.2:c.2685+423_2685+436dup NP_001335873.1:n.2685+423_2685+436dup
NM_001348945.2:c.2895+423_2895+436dup NP_001335874.1:n.2895+423_2895+436dup