Canonical Allele Identifier: CA2683605499
Gene: ABCB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87516814_87516818del , CM000669.2:g.87516814_87516818del GRCh38
NC_000007.13:g.87146130_87146134del , CM000669.1:g.87146130_87146134del GRCh37
NC_000007.12:g.86984066_86984070del NCBI36
NG_011513.1:g.201431_201435del

Transcript Alleles

HGVS Amino-acid Change
ENST00000265724.8:c.2928-153_2928-149del ENSP00000265724.3:n.2928-153_2928-149del
ENST00000622132.5:c.2928-153_2928-149del MANE Select ENSP00000478255.1:n.2928-153_2928-149del
ENST00000265724.7:c.2928-153_2928-149del ENSP00000265724.3:n.2928-153_2928-149del
ENST00000475929.5:n.84-153_84-149del
ENST00000483831.1:n.486-153_486-149del
ENST00000488737.6:n.570-153_570-149del
ENST00000496821.5:n.556-153_556-149del
ENST00000543898.5:c.2736-153_2736-149del ENSP00000444095.1:n.2736-153_2736-149del
ENST00000622132.4:c.2928-153_2928-149del ENSP00000478255.1:n.2928-153_2928-149del
NM_000927.4:c.2928-153_2928-149del NP_000918.2:n.2928-153_2928-149del
NM_001348944.1:c.2928-153_2928-149del NP_001335873.1:n.2928-153_2928-149del
NM_001348945.1:c.3138-153_3138-149del NP_001335874.1:n.3138-153_3138-149del
NM_001348946.1:c.2928-153_2928-149del NP_001335875.1:n.2928-153_2928-149del
NM_001348946.2:c.2928-153_2928-149del MANE Select NP_001335875.1:n.2928-153_2928-149del
NM_000927.5:c.2928-153_2928-149del NP_000918.2:n.2928-153_2928-149del
NM_001348944.2:c.2928-153_2928-149del NP_001335873.1:n.2928-153_2928-149del
NM_001348945.2:c.3138-153_3138-149del NP_001335874.1:n.3138-153_3138-149del