Canonical Allele Identifier: CA1723630648

Gene: ABCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87536069_87536070delinsAG , CM000669.2:g.87536069_87536070delinsAG	GRCh38
NC_000007.13:g.87165385_87165386delinsAG , CM000669.1:g.87165385_87165386delinsAG	GRCh37
NC_000007.12:g.87003321_87003322delinsAG	NCBI36
NG_011513.1:g.182179_182180delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.2481+388_2481+389delinsCT	ENSP00000265724.3:n.2481+388_2481+389delinsCT
ENST00000622132.5:c.2481+388_2481+389delinsCT MANE Select	ENSP00000478255.1:n.2481+388_2481+389delinsCT
ENST00000265724.7:c.2481+388_2481+389delinsCT	ENSP00000265724.3:n.2481+388_2481+389delinsCT
ENST00000496821.5:n.109+388_109+389delinsCT
ENST00000543898.5:c.2289+388_2289+389delinsCT	ENSP00000444095.1:n.2289+388_2289+389delinsCT
ENST00000622132.4:c.2481+388_2481+389delinsCT	ENSP00000478255.1:n.2481+388_2481+389delinsCT
NM_000927.4:c.2481+388_2481+389delinsCT	NP_000918.2:n.2481+388_2481+389delinsCT
NM_001348944.1:c.2481+388_2481+389delinsCT	NP_001335873.1:n.2481+388_2481+389delinsCT
NM_001348945.1:c.2691+388_2691+389delinsCT	NP_001335874.1:n.2691+388_2691+389delinsCT
NM_001348946.1:c.2481+388_2481+389delinsCT	NP_001335875.1:n.2481+388_2481+389delinsCT
NM_001348946.2:c.2481+388_2481+389delinsCT MANE Select	NP_001335875.1:n.2481+388_2481+389delinsCT
NM_000927.5:c.2481+388_2481+389delinsCT	NP_000918.2:n.2481+388_2481+389delinsCT
NM_001348944.2:c.2481+388_2481+389delinsCT	NP_001335873.1:n.2481+388_2481+389delinsCT
NM_001348945.2:c.2691+388_2691+389delinsCT	NP_001335874.1:n.2691+388_2691+389delinsCT