Canonical Allele Identifier: CA1723631015

Gene: ABCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87536226_87536230delinsCATGA , CM000669.2:g.87536226_87536230delinsCATGA	GRCh38
NC_000007.13:g.87165542_87165546delinsCATGA , CM000669.1:g.87165542_87165546delinsCATGA	GRCh37
NC_000007.12:g.87003478_87003482delinsCATGA	NCBI36
NG_011513.1:g.182019_182023delinsTCATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.2481+228_2481+232delinsTCATG	ENSP00000265724.3:n.2481+228_2481+232delinsTCATG
ENST00000622132.5:c.2481+228_2481+232delinsTCATG MANE Select	ENSP00000478255.1:n.2481+228_2481+232delinsTCATG
ENST00000265724.7:c.2481+228_2481+232delinsTCATG	ENSP00000265724.3:n.2481+228_2481+232delinsTCATG
ENST00000496821.5:n.109+228_109+232delinsTCATG
ENST00000543898.5:c.2289+228_2289+232delinsTCATG	ENSP00000444095.1:n.2289+228_2289+232delinsTCATG
ENST00000622132.4:c.2481+228_2481+232delinsTCATG	ENSP00000478255.1:n.2481+228_2481+232delinsTCATG
NM_000927.4:c.2481+228_2481+232delinsTCATG	NP_000918.2:n.2481+228_2481+232delinsTCATG
NM_001348944.1:c.2481+228_2481+232delinsTCATG	NP_001335873.1:n.2481+228_2481+232delinsTCATG
NM_001348945.1:c.2691+228_2691+232delinsTCATG	NP_001335874.1:n.2691+228_2691+232delinsTCATG
NM_001348946.1:c.2481+228_2481+232delinsTCATG	NP_001335875.1:n.2481+228_2481+232delinsTCATG
NM_001348946.2:c.2481+228_2481+232delinsTCATG MANE Select	NP_001335875.1:n.2481+228_2481+232delinsTCATG
NM_000927.5:c.2481+228_2481+232delinsTCATG	NP_000918.2:n.2481+228_2481+232delinsTCATG
NM_001348944.2:c.2481+228_2481+232delinsTCATG	NP_001335873.1:n.2481+228_2481+232delinsTCATG
NM_001348945.2:c.2691+228_2691+232delinsTCATG	NP_001335874.1:n.2691+228_2691+232delinsTCATG