Canonical Allele Identifier: CA1723631397

Gene: ABCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87530854_87530857delinsAAAG , CM000669.2:g.87530854_87530857delinsAAAG	GRCh38
NC_000007.13:g.87160170_87160173delinsAAAG , CM000669.1:g.87160170_87160173delinsAAAG	GRCh37
NC_000007.12:g.86998106_86998109delinsAAAG	NCBI36
NG_011513.1:g.187392_187395delinsCTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.2685+437_2685+440delinsCTTT	ENSP00000265724.3:n.2685+437_2685+440delinsCTTT
ENST00000622132.5:c.2685+437_2685+440delinsCTTT MANE Select	ENSP00000478255.1:n.2685+437_2685+440delinsCTTT
ENST00000265724.7:c.2685+437_2685+440delinsCTTT	ENSP00000265724.3:n.2685+437_2685+440delinsCTTT
ENST00000488737.6:n.327+437_327+440delinsCTTT
ENST00000496821.5:n.313+437_313+440delinsCTTT
ENST00000543898.5:c.2493+437_2493+440delinsCTTT	ENSP00000444095.1:n.2493+437_2493+440delinsCTTT
ENST00000622132.4:c.2685+437_2685+440delinsCTTT	ENSP00000478255.1:n.2685+437_2685+440delinsCTTT
NM_000927.4:c.2685+437_2685+440delinsCTTT	NP_000918.2:n.2685+437_2685+440delinsCTTT
NM_001348944.1:c.2685+437_2685+440delinsCTTT	NP_001335873.1:n.2685+437_2685+440delinsCTTT
NM_001348945.1:c.2895+437_2895+440delinsCTTT	NP_001335874.1:n.2895+437_2895+440delinsCTTT
NM_001348946.1:c.2685+437_2685+440delinsCTTT	NP_001335875.1:n.2685+437_2685+440delinsCTTT
NM_001348946.2:c.2685+437_2685+440delinsCTTT MANE Select	NP_001335875.1:n.2685+437_2685+440delinsCTTT
NM_000927.5:c.2685+437_2685+440delinsCTTT	NP_000918.2:n.2685+437_2685+440delinsCTTT
NM_001348944.2:c.2685+437_2685+440delinsCTTT	NP_001335873.1:n.2685+437_2685+440delinsCTTT
NM_001348945.2:c.2895+437_2895+440delinsCTTT	NP_001335874.1:n.2895+437_2895+440delinsCTTT