Canonical Allele Identifier: CA1723631371

Gene: ABCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87530849_87530852delinsGAAA , CM000669.2:g.87530849_87530852delinsGAAA	GRCh38
NC_000007.13:g.87160165_87160168delinsGAAA , CM000669.1:g.87160165_87160168delinsGAAA	GRCh37
NC_000007.12:g.86998101_86998104delinsGAAA	NCBI36
NG_011513.1:g.187397_187400delinsTTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.2685+442_2685+445delinsTTTC	ENSP00000265724.3:n.2685+442_2685+445delinsTTTC
ENST00000622132.5:c.2685+442_2685+445delinsTTTC MANE Select	ENSP00000478255.1:n.2685+442_2685+445delinsTTTC
ENST00000265724.7:c.2685+442_2685+445delinsTTTC	ENSP00000265724.3:n.2685+442_2685+445delinsTTTC
ENST00000488737.6:n.327+442_327+445delinsTTTC
ENST00000496821.5:n.313+442_313+445delinsTTTC
ENST00000543898.5:c.2493+442_2493+445delinsTTTC	ENSP00000444095.1:n.2493+442_2493+445delinsTTTC
ENST00000622132.4:c.2685+442_2685+445delinsTTTC	ENSP00000478255.1:n.2685+442_2685+445delinsTTTC
NM_000927.4:c.2685+442_2685+445delinsTTTC	NP_000918.2:n.2685+442_2685+445delinsTTTC
NM_001348944.1:c.2685+442_2685+445delinsTTTC	NP_001335873.1:n.2685+442_2685+445delinsTTTC
NM_001348945.1:c.2895+442_2895+445delinsTTTC	NP_001335874.1:n.2895+442_2895+445delinsTTTC
NM_001348946.1:c.2685+442_2685+445delinsTTTC	NP_001335875.1:n.2685+442_2685+445delinsTTTC
NM_001348946.2:c.2685+442_2685+445delinsTTTC MANE Select	NP_001335875.1:n.2685+442_2685+445delinsTTTC
NM_000927.5:c.2685+442_2685+445delinsTTTC	NP_000918.2:n.2685+442_2685+445delinsTTTC
NM_001348944.2:c.2685+442_2685+445delinsTTTC	NP_001335873.1:n.2685+442_2685+445delinsTTTC
NM_001348945.2:c.2895+442_2895+445delinsTTTC	NP_001335874.1:n.2895+442_2895+445delinsTTTC