Canonical Allele Identifier: CA2683605741

Gene: ABCB1

Linked Data

• gnomAD v4: 7-87531258-CTACTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87531259_87531263del , CM000669.2:g.87531259_87531263del	GRCh38
NC_000007.13:g.87160575_87160579del , CM000669.1:g.87160575_87160579del	GRCh37
NC_000007.12:g.86998511_86998515del	NCBI36
NG_011513.1:g.186986_186990del

Transcript Alleles

HGVS	Amino-acid change
ENST00000265724.8:c.2685+31_2685+35del	ENSP00000265724.3:n.2685+31_2685+35del
ENST00000622132.5:c.2685+31_2685+35del MANE Select	ENSP00000478255.1:n.2685+31_2685+35del
ENST00000265724.7:c.2685+31_2685+35del	ENSP00000265724.3:n.2685+31_2685+35del
ENST00000488737.6:n.327+31_327+35del
ENST00000496821.5:n.313+31_313+35del
ENST00000543898.5:c.2493+31_2493+35del	ENSP00000444095.1:n.2493+31_2493+35del
ENST00000622132.4:c.2685+31_2685+35del	ENSP00000478255.1:n.2685+31_2685+35del
NM_000927.4:c.2685+31_2685+35del	NP_000918.2:n.2685+31_2685+35del
NM_001348944.1:c.2685+31_2685+35del	NP_001335873.1:n.2685+31_2685+35del
NM_001348945.1:c.2895+31_2895+35del	NP_001335874.1:n.2895+31_2895+35del
NM_001348946.1:c.2685+31_2685+35del	NP_001335875.1:n.2685+31_2685+35del
NM_001348946.2:c.2685+31_2685+35del MANE Select	NP_001335875.1:n.2685+31_2685+35del
NM_000927.5:c.2685+31_2685+35del	NP_000918.2:n.2685+31_2685+35del
NM_001348944.2:c.2685+31_2685+35del	NP_001335873.1:n.2685+31_2685+35del
NM_001348945.2:c.2895+31_2895+35del	NP_001335874.1:n.2895+31_2895+35del