Canonical Allele Identifier: CA162110648
Gene: ABCB1 HGNC NCBI

Linked Data

dbSNP Id: rs972401993

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87530949_87530952del , CM000669.2:g.87530949_87530952del GRCh38
NC_000007.13:g.87160265_87160268del , CM000669.1:g.87160265_87160268del GRCh37
NC_000007.12:g.86998201_86998204del NCBI36
NG_011513.1:g.187308_187311del

Transcript Alleles

HGVS Amino-acid Change
ENST00000265724.8:c.2685+353_2685+356del ENSP00000265724.3:n.2685+353_2685+356del
ENST00000622132.5:c.2685+353_2685+356del MANE Select ENSP00000478255.1:n.2685+353_2685+356del
ENST00000265724.7:c.2685+353_2685+356del ENSP00000265724.3:n.2685+353_2685+356del
ENST00000488737.6:n.327+353_327+356del
ENST00000496821.5:n.313+353_313+356del
ENST00000543898.5:c.2493+353_2493+356del ENSP00000444095.1:n.2493+353_2493+356del
ENST00000622132.4:c.2685+353_2685+356del ENSP00000478255.1:n.2685+353_2685+356del
NM_000927.4:c.2685+353_2685+356del NP_000918.2:n.2685+353_2685+356del
NM_001348944.1:c.2685+353_2685+356del NP_001335873.1:n.2685+353_2685+356del
NM_001348945.1:c.2895+353_2895+356del NP_001335874.1:n.2895+353_2895+356del
NM_001348946.1:c.2685+353_2685+356del NP_001335875.1:n.2685+353_2685+356del
NM_001348946.2:c.2685+353_2685+356del MANE Select NP_001335875.1:n.2685+353_2685+356del
NM_000927.5:c.2685+353_2685+356del NP_000918.2:n.2685+353_2685+356del
NM_001348944.2:c.2685+353_2685+356del NP_001335873.1:n.2685+353_2685+356del
NM_001348945.2:c.2895+353_2895+356del NP_001335874.1:n.2895+353_2895+356del