Canonical Allele Identifier: CA1723630709

Gene: ABCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87551498_87551499delinsTA , CM000669.2:g.87551498_87551499delinsTA	GRCh38
NC_000007.13:g.87180814_87180815delinsTA , CM000669.1:g.87180814_87180815delinsTA	GRCh37
NC_000007.12:g.87018750_87018751delinsTA	NCBI36
NG_011513.1:g.166750_166751delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.1000-661_1000-660delinsTA	ENSP00000265724.3:n.1000-661_1000-660delinsTA
ENST00000622132.5:c.1000-661_1000-660delinsTA MANE Select	ENSP00000478255.1:n.1000-661_1000-660delinsTA
ENST00000265724.7:c.1000-661_1000-660delinsTA	ENSP00000265724.3:n.1000-661_1000-660delinsTA
ENST00000543898.5:c.808-661_808-660delinsTA	ENSP00000444095.1:n.808-661_808-660delinsTA
ENST00000622132.4:c.1000-661_1000-660delinsTA	ENSP00000478255.1:n.1000-661_1000-660delinsTA
NM_000927.4:c.1000-661_1000-660delinsTA	NP_000918.2:n.1000-661_1000-660delinsTA
NM_001348944.1:c.1000-661_1000-660delinsTA	NP_001335873.1:n.1000-661_1000-660delinsTA
NM_001348945.1:c.1210-661_1210-660delinsTA	NP_001335874.1:n.1210-661_1210-660delinsTA
NM_001348946.1:c.1000-661_1000-660delinsTA	NP_001335875.1:n.1000-661_1000-660delinsTA
NM_001348946.2:c.1000-661_1000-660delinsTA MANE Select	NP_001335875.1:n.1000-661_1000-660delinsTA
NM_000927.5:c.1000-661_1000-660delinsTA	NP_000918.2:n.1000-661_1000-660delinsTA
NM_001348944.2:c.1000-661_1000-660delinsTA	NP_001335873.1:n.1000-661_1000-660delinsTA
NM_001348945.2:c.1210-661_1210-660delinsTA	NP_001335874.1:n.1210-661_1210-660delinsTA