Canonical Allele Identifier: CA2776827305

Gene: ABCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87520672del , CM000669.2:g.87520672del	GRCh38
NC_000007.13:g.87149988del , CM000669.1:g.87149988del	GRCh37
NC_000007.12:g.86987924del	NCBI36
NG_011513.1:g.197579del

Transcript Alleles

HGVS	Amino-acid change
ENST00000265724.8:c.2786+106del	ENSP00000265724.3:n.2786+106del
ENST00000622132.5:c.2786+106del MANE Select	ENSP00000478255.1:n.2786+106del
ENST00000265724.7:c.2786+106del	ENSP00000265724.3:n.2786+106del
ENST00000483831.1:n.344+106del
ENST00000488737.6:n.428+106del
ENST00000496821.5:n.414+106del
ENST00000543898.5:c.2594+106del	ENSP00000444095.1:n.2594+106del
ENST00000622132.4:c.2786+106del	ENSP00000478255.1:n.2786+106del
NM_000927.4:c.2786+106del	NP_000918.2:n.2786+106del
NM_001348944.1:c.2786+106del	NP_001335873.1:n.2786+106del
NM_001348945.1:c.2996+106del	NP_001335874.1:n.2996+106del
NM_001348946.1:c.2786+106del	NP_001335875.1:n.2786+106del
NM_001348946.2:c.2786+106del MANE Select	NP_001335875.1:n.2786+106del
NM_000927.5:c.2786+106del	NP_000918.2:n.2786+106del
NM_001348944.2:c.2786+106del	NP_001335873.1:n.2786+106del
NM_001348945.2:c.2996+106del	NP_001335874.1:n.2996+106del