Canonical Allele Identifier: CA2776826000

Gene: ABCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87545150_87545152del , CM000669.2:g.87545150_87545152del	GRCh38
NC_000007.13:g.87174466_87174468del , CM000669.1:g.87174466_87174468del	GRCh37
NC_000007.12:g.87012402_87012404del	NCBI36
NG_011513.1:g.173097_173099del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.1888-153_1888-151del	ENSP00000265724.3:n.1888-153_1888-151del
ENST00000622132.5:c.1888-153_1888-151del MANE Select	ENSP00000478255.1:n.1888-153_1888-151del
ENST00000265724.7:c.1888-153_1888-151del	ENSP00000265724.3:n.1888-153_1888-151del
ENST00000543898.5:c.1696-153_1696-151del	ENSP00000444095.1:n.1696-153_1696-151del
ENST00000622132.4:c.1888-153_1888-151del	ENSP00000478255.1:n.1888-153_1888-151del
NM_000927.4:c.1888-153_1888-151del	NP_000918.2:n.1888-153_1888-151del
NM_001348944.1:c.1888-153_1888-151del	NP_001335873.1:n.1888-153_1888-151del
NM_001348945.1:c.2098-153_2098-151del	NP_001335874.1:n.2098-153_2098-151del
NM_001348946.1:c.1888-153_1888-151del	NP_001335875.1:n.1888-153_1888-151del
NM_001348946.2:c.1888-153_1888-151del MANE Select	NP_001335875.1:n.1888-153_1888-151del
NM_000927.5:c.1888-153_1888-151del	NP_000918.2:n.1888-153_1888-151del
NM_001348944.2:c.1888-153_1888-151del	NP_001335873.1:n.1888-153_1888-151del
NM_001348945.2:c.2098-153_2098-151del	NP_001335874.1:n.2098-153_2098-151del