Canonical Allele Identifier: CA843378757

Gene: ABCB1

Linked Data

• dbSNP Id: rs1401110556
• MyVariant Identifiers: chr7:g.87160154_87160163del (hg19) ; chr7:g.87530838_87530847del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87530838_87530847del , CM000669.2:g.87530838_87530847del	GRCh38
NC_000007.13:g.87160154_87160163del , CM000669.1:g.87160154_87160163del	GRCh37
NC_000007.12:g.86998090_86998099del	NCBI36
NG_011513.1:g.187402_187411del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.2685+447_2685+456del	ENSP00000265724.3:n.2685+447_2685+456del
ENST00000622132.5:c.2685+447_2685+456del MANE Select	ENSP00000478255.1:n.2685+447_2685+456del
ENST00000265724.7:c.2685+447_2685+456del	ENSP00000265724.3:n.2685+447_2685+456del
ENST00000488737.6:n.327+447_327+456del
ENST00000496821.5:n.313+447_313+456del
ENST00000543898.5:c.2493+447_2493+456del	ENSP00000444095.1:n.2493+447_2493+456del
ENST00000622132.4:c.2685+447_2685+456del	ENSP00000478255.1:n.2685+447_2685+456del
NM_000927.4:c.2685+447_2685+456del	NP_000918.2:n.2685+447_2685+456del
NM_001348944.1:c.2685+447_2685+456del	NP_001335873.1:n.2685+447_2685+456del
NM_001348945.1:c.2895+447_2895+456del	NP_001335874.1:n.2895+447_2895+456del
NM_001348946.1:c.2685+447_2685+456del	NP_001335875.1:n.2685+447_2685+456del
NM_001348946.2:c.2685+447_2685+456del MANE Select	NP_001335875.1:n.2685+447_2685+456del
NM_000927.5:c.2685+447_2685+456del	NP_000918.2:n.2685+447_2685+456del
NM_001348944.2:c.2685+447_2685+456del	NP_001335873.1:n.2685+447_2685+456del
NM_001348945.2:c.2895+447_2895+456del	NP_001335874.1:n.2895+447_2895+456del