Canonical Allele Identifier: CA1723628610

Gene: ABCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87520729_87520730delinsAT , CM000669.2:g.87520729_87520730delinsAT	GRCh38
NC_000007.13:g.87150045_87150046delinsAT , CM000669.1:g.87150045_87150046delinsAT	GRCh37
NC_000007.12:g.86987981_86987982delinsAT	NCBI36
NG_011513.1:g.197519_197520delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.2786+46_2786+47delinsAT	ENSP00000265724.3:n.2786+46_2786+47delinsAT
ENST00000622132.5:c.2786+46_2786+47delinsAT MANE Select	ENSP00000478255.1:n.2786+46_2786+47delinsAT
ENST00000265724.7:c.2786+46_2786+47delinsAT	ENSP00000265724.3:n.2786+46_2786+47delinsAT
ENST00000483831.1:n.344+46_344+47delinsAT
ENST00000488737.6:n.428+46_428+47delinsAT
ENST00000496821.5:n.414+46_414+47delinsAT
ENST00000543898.5:c.2594+46_2594+47delinsAT	ENSP00000444095.1:n.2594+46_2594+47delinsAT
ENST00000622132.4:c.2786+46_2786+47delinsAT	ENSP00000478255.1:n.2786+46_2786+47delinsAT
NM_000927.4:c.2786+46_2786+47delinsAT	NP_000918.2:n.2786+46_2786+47delinsAT
NM_001348944.1:c.2786+46_2786+47delinsAT	NP_001335873.1:n.2786+46_2786+47delinsAT
NM_001348945.1:c.2996+46_2996+47delinsAT	NP_001335874.1:n.2996+46_2996+47delinsAT
NM_001348946.1:c.2786+46_2786+47delinsAT	NP_001335875.1:n.2786+46_2786+47delinsAT
NM_001348946.2:c.2786+46_2786+47delinsAT MANE Select	NP_001335875.1:n.2786+46_2786+47delinsAT
NM_000927.5:c.2786+46_2786+47delinsAT	NP_000918.2:n.2786+46_2786+47delinsAT
NM_001348944.2:c.2786+46_2786+47delinsAT	NP_001335873.1:n.2786+46_2786+47delinsAT
NM_001348945.2:c.2996+46_2996+47delinsAT	NP_001335874.1:n.2996+46_2996+47delinsAT