Canonical Allele Identifier: CA1723628603

Gene: ABCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87520710_87520711delinsTC , CM000669.2:g.87520710_87520711delinsTC	GRCh38
NC_000007.13:g.87150026_87150027delinsTC , CM000669.1:g.87150026_87150027delinsTC	GRCh37
NC_000007.12:g.86987962_86987963delinsTC	NCBI36
NG_011513.1:g.197538_197539delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.2786+65_2786+66delinsGA	ENSP00000265724.3:n.2786+65_2786+66delinsGA
ENST00000622132.5:c.2786+65_2786+66delinsGA MANE Select	ENSP00000478255.1:n.2786+65_2786+66delinsGA
ENST00000265724.7:c.2786+65_2786+66delinsGA	ENSP00000265724.3:n.2786+65_2786+66delinsGA
ENST00000483831.1:n.344+65_344+66delinsGA
ENST00000488737.6:n.428+65_428+66delinsGA
ENST00000496821.5:n.414+65_414+66delinsGA
ENST00000543898.5:c.2594+65_2594+66delinsGA	ENSP00000444095.1:n.2594+65_2594+66delinsGA
ENST00000622132.4:c.2786+65_2786+66delinsGA	ENSP00000478255.1:n.2786+65_2786+66delinsGA
NM_000927.4:c.2786+65_2786+66delinsGA	NP_000918.2:n.2786+65_2786+66delinsGA
NM_001348944.1:c.2786+65_2786+66delinsGA	NP_001335873.1:n.2786+65_2786+66delinsGA
NM_001348945.1:c.2996+65_2996+66delinsGA	NP_001335874.1:n.2996+65_2996+66delinsGA
NM_001348946.1:c.2786+65_2786+66delinsGA	NP_001335875.1:n.2786+65_2786+66delinsGA
NM_001348946.2:c.2786+65_2786+66delinsGA MANE Select	NP_001335875.1:n.2786+65_2786+66delinsGA
NM_000927.5:c.2786+65_2786+66delinsGA	NP_000918.2:n.2786+65_2786+66delinsGA
NM_001348944.2:c.2786+65_2786+66delinsGA	NP_001335873.1:n.2786+65_2786+66delinsGA
NM_001348945.2:c.2996+65_2996+66delinsGA	NP_001335874.1:n.2996+65_2996+66delinsGA