Canonical Allele Identifier: CA2776827946

Gene: ABCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87600167_87600168insACG , CM000669.2:g.87600167_87600168insACG	GRCh38
NC_000007.13:g.87229483_87229484insACG , CM000669.1:g.87229483_87229484insACG	GRCh37
NC_000007.12:g.87067419_87067420insACG	NCBI36
NG_011513.1:g.118082_118083insGTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.18_19insGTC	ENSP00000265724.3:p.Asp6_Arg7insVal
ENST00000622132.5:c.18_19insGTC MANE Select	ENSP00000478255.1:p.Asp6_Arg7insVal
ENST00000265724.7:c.18_19insGTC	ENSP00000265724.3:p.Asp6_Arg7insVal
ENST00000416177.1:c.18_19insGTC	ENSP00000399419.1:p.Asp6_Arg7insVal
ENST00000543898.5:c.18_19insGTC	ENSP00000444095.1:p.Asp6_Arg7insVal
ENST00000622132.4:c.18_19insGTC	ENSP00000478255.1:p.Asp6_Arg7insVal
NM_000927.4:c.18_19insGTC	NP_000918.2:p.Asp6_Arg7insVal
NM_001348944.1:c.18_19insGTC	NP_001335873.1:p.Asp6_Arg7insVal
NM_001348945.1:c.228_229insGTC	NP_001335874.1:p.Asp76_Arg77insVal
NM_001348946.1:c.18_19insGTC	NP_001335875.1:p.Asp6_Arg7insVal
NM_001348946.2:c.18_19insGTC MANE Select	NP_001335875.1:p.Asp6_Arg7insVal
NM_000927.5:c.18_19insGTC	NP_000918.2:p.Asp6_Arg7insVal
NM_001348944.2:c.18_19insGTC	NP_001335873.1:p.Asp6_Arg7insVal
NM_001348945.2:c.228_229insGTC	NP_001335874.1:p.Asp76_Arg77insVal