Canonical Allele Identifier: CA1723631022

Gene: ABCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87530806_87530846delinsCAAGAAAGCAAGAAAGCAAGAAAGCAAGAAAGCAAGAAAGA , CM000669.2:g.87530806_87530846delinsCAAGAAAGCAAGAAAGCAAGAAAGCAAGAAAGCAAGAAAGA	GRCh38
NC_000007.13:g.87160122_87160162delinsCAAGAAAGCAAGAAAGCAAGAAAGCAAGAAAGCAAGAAAGA , CM000669.1:g.87160122_87160162delinsCAAGAAAGCAAGAAAGCAAGAAAGCAAGAAAGCAAGAAAGA	GRCh37
NC_000007.12:g.86998058_86998098delinsCAAGAAAGCAAGAAAGCAAGAAAGCAAGAAAGCAAGAAAGA	NCBI36
NG_011513.1:g.187403_187443delinsTCTTTCTTGCTTTCTTGCTTTCTTGCTTTCTTGCTTTCTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.2685+448_2685+488delinsTCTTTCTTGCTTTCTTGCTTTCTTGCTTTCTTGCTTTCTTG	ENSP00000265724.3:n.2685+448_2685+488delinsTCTTTCTTGCTTTCTTGC...
ENST00000622132.5:c.2685+448_2685+488delinsTCTTTCTTGCTTTCTTGCTTTCTTGCTTTCTTGCTTTCTTG MANE Select	ENSP00000478255.1:n.2685+448_2685+488delinsTCTTTCTTGCTTTCTTGC...
ENST00000265724.7:c.2685+448_2685+488delinsTCTTTCTTGCTTTCTTGCTTTCTTGCTTTCTTGCTTTCTTG	ENSP00000265724.3:n.2685+448_2685+488delinsTCTTTCTTGCTTTCTTGC...
ENST00000488737.6:n.327+448_327+488delinsTCTTTCTTGCTTTCTTGCTTTCTTGCTTTCTTGCTTTCTTG
ENST00000496821.5:n.313+448_313+488delinsTCTTTCTTGCTTTCTTGCTTTCTTGCTTTCTTGCTTTCTTG
ENST00000543898.5:c.2493+448_2493+488delinsTCTTTCTTGCTTTCTTGCTTTCTTGCTTTCTTGCTTTCTTG	ENSP00000444095.1:n.2493+448_2493+488delinsTCTTTCTTGCTTTCTTGC...
ENST00000622132.4:c.2685+448_2685+488delinsTCTTTCTTGCTTTCTTGCTTTCTTGCTTTCTTGCTTTCTTG	ENSP00000478255.1:n.2685+448_2685+488delinsTCTTTCTTGCTTTCTTGC...
NM_000927.4:c.2685+448_2685+488delinsTCTTTCTTGCTTTCTTGCTTTCTTGCTTTCTTGCTTTCTTG	NP_000918.2:n.2685+448_2685+488delinsTCTTTCTTGCTTTCTTGCTTTCTT...
NM_001348944.1:c.2685+448_2685+488delinsTCTTTCTTGCTTTCTTGCTTTCTTGCTTTCTTGCTTTCTTG	NP_001335873.1:n.2685+448_2685+488delinsTCTTTCTTGCTTTCTTGCTTT...
NM_001348945.1:c.2895+448_2895+488delinsTCTTTCTTGCTTTCTTGCTTTCTTGCTTTCTTGCTTTCTTG	NP_001335874.1:n.2895+448_2895+488delinsTCTTTCTTGCTTTCTTGCTTT...
NM_001348946.1:c.2685+448_2685+488delinsTCTTTCTTGCTTTCTTGCTTTCTTGCTTTCTTGCTTTCTTG	NP_001335875.1:n.2685+448_2685+488delinsTCTTTCTTGCTTTCTTGCTTT...
NM_001348946.2:c.2685+448_2685+488delinsTCTTTCTTGCTTTCTTGCTTTCTTGCTTTCTTGCTTTCTTG MANE Select	NP_001335875.1:n.2685+448_2685+488delinsTCTTTCTTGCTTTCTTGCTTT...
NM_000927.5:c.2685+448_2685+488delinsTCTTTCTTGCTTTCTTGCTTTCTTGCTTTCTTGCTTTCTTG	NP_000918.2:n.2685+448_2685+488delinsTCTTTCTTGCTTTCTTGCTTTCTT...
NM_001348944.2:c.2685+448_2685+488delinsTCTTTCTTGCTTTCTTGCTTTCTTGCTTTCTTGCTTTCTTG	NP_001335873.1:n.2685+448_2685+488delinsTCTTTCTTGCTTTCTTGCTTT...
NM_001348945.2:c.2895+448_2895+488delinsTCTTTCTTGCTTTCTTGCTTTCTTGCTTTCTTGCTTTCTTG	NP_001335874.1:n.2895+448_2895+488delinsTCTTTCTTGCTTTCTTGCTTT...