Canonical Allele Identifier: CA1723631507

Gene: ABCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87530871_87530873delinsAAG , CM000669.2:g.87530871_87530873delinsAAG	GRCh38
NC_000007.13:g.87160187_87160189delinsAAG , CM000669.1:g.87160187_87160189delinsAAG	GRCh37
NC_000007.12:g.86998123_86998125delinsAAG	NCBI36
NG_011513.1:g.187376_187378delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
NM_001348946.2:c.2685+421_2685+423delinsCTT MANE Select	NP_001335875.1:n.2685+421_2685+423delinsCTT
ENST00000622132.5:c.2685+421_2685+423delinsCTT MANE Select	ENSP00000478255.1:n.2685+421_2685+423delinsCTT
NM_000927.4:c.2685+421_2685+423delinsCTT	NP_000918.2:n.2685+421_2685+423delinsCTT
NM_000927.5:c.2685+421_2685+423delinsCTT	NP_000918.2:n.2685+421_2685+423delinsCTT
NM_001348944.1:c.2685+421_2685+423delinsCTT	NP_001335873.1:n.2685+421_2685+423delinsCTT
NM_001348944.2:c.2685+421_2685+423delinsCTT	NP_001335873.1:n.2685+421_2685+423delinsCTT
NM_001348945.1:c.2895+421_2895+423delinsCTT	NP_001335874.1:n.2895+421_2895+423delinsCTT
NM_001348945.2:c.2895+421_2895+423delinsCTT	NP_001335874.1:n.2895+421_2895+423delinsCTT
NM_001348946.1:c.2685+421_2685+423delinsCTT	NP_001335875.1:n.2685+421_2685+423delinsCTT
ENST00000265724.7:c.2685+421_2685+423delinsCTT	ENSP00000265724.3:n.2685+421_2685+423delinsCTT
ENST00000265724.8:c.2685+421_2685+423delinsCTT	ENSP00000265724.3:n.2685+421_2685+423delinsCTT
ENST00000488737.6:n.327+421_327+423delinsCTT
ENST00000496821.5:n.313+421_313+423delinsCTT
ENST00000543898.5:c.2493+421_2493+423delinsCTT	ENSP00000444095.1:n.2493+421_2493+423delinsCTT
ENST00000622132.4:c.2685+421_2685+423delinsCTT	ENSP00000478255.1:n.2685+421_2685+423delinsCTT