Canonical Allele Identifier: CA2683605111
Gene: ABCB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87515088_87515090dup , CM000669.2:g.87515088_87515090dup GRCh38
NC_000007.13:g.87144404_87144406dup , CM000669.1:g.87144404_87144406dup GRCh37
NC_000007.12:g.86982340_86982342dup NCBI36
NG_011513.1:g.203160_203162dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000265724.8:c.3282+142_3282+144dup ENSP00000265724.3:n.3282+142_3282+144dup
ENST00000622132.5:c.3282+142_3282+144dup MANE Select ENSP00000478255.1:n.3282+142_3282+144dup
ENST00000265724.7:c.3282+142_3282+144dup ENSP00000265724.3:n.3282+142_3282+144dup
ENST00000475929.5:n.438+142_438+144dup
ENST00000488737.6:n.924+142_924+144dup
ENST00000543898.5:c.3090+142_3090+144dup ENSP00000444095.1:n.3090+142_3090+144dup
ENST00000622132.4:c.3282+142_3282+144dup ENSP00000478255.1:n.3282+142_3282+144dup
NM_000927.4:c.3282+142_3282+144dup NP_000918.2:n.3282+142_3282+144dup
NM_001348944.1:c.3282+142_3282+144dup NP_001335873.1:n.3282+142_3282+144dup
NM_001348945.1:c.3492+142_3492+144dup NP_001335874.1:n.3492+142_3492+144dup
NM_001348946.1:c.3282+142_3282+144dup NP_001335875.1:n.3282+142_3282+144dup
NM_001348946.2:c.3282+142_3282+144dup MANE Select NP_001335875.1:n.3282+142_3282+144dup
NM_000927.5:c.3282+142_3282+144dup NP_000918.2:n.3282+142_3282+144dup
NM_001348944.2:c.3282+142_3282+144dup NP_001335873.1:n.3282+142_3282+144dup
NM_001348945.2:c.3492+142_3492+144dup NP_001335874.1:n.3492+142_3492+144dup