Canonical Allele Identifier: CA1723599194

Gene: ABCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87522620_87522621delinsCT , CM000669.2:g.87522620_87522621delinsCT	GRCh38
NC_000007.13:g.87151936_87151937delinsCT , CM000669.1:g.87151936_87151937delinsCT	GRCh37
NC_000007.12:g.86989872_86989873delinsCT	NCBI36
NG_011513.1:g.195628_195629delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.2686-1745_2686-1744delinsAG	ENSP00000265724.3:n.2686-1745_2686-1744delinsAG
ENST00000622132.5:c.2686-1745_2686-1744delinsAG MANE Select	ENSP00000478255.1:n.2686-1745_2686-1744delinsAG
ENST00000265724.7:c.2686-1745_2686-1744delinsAG	ENSP00000265724.3:n.2686-1745_2686-1744delinsAG
ENST00000488737.6:n.328-1745_328-1744delinsAG
ENST00000496821.5:n.314-1745_314-1744delinsAG
ENST00000543898.5:c.2494-1745_2494-1744delinsAG	ENSP00000444095.1:n.2494-1745_2494-1744delinsAG
ENST00000622132.4:c.2686-1745_2686-1744delinsAG	ENSP00000478255.1:n.2686-1745_2686-1744delinsAG
NM_000927.4:c.2686-1745_2686-1744delinsAG	NP_000918.2:n.2686-1745_2686-1744delinsAG
NM_001348944.1:c.2686-1745_2686-1744delinsAG	NP_001335873.1:n.2686-1745_2686-1744delinsAG
NM_001348945.1:c.2896-1745_2896-1744delinsAG	NP_001335874.1:n.2896-1745_2896-1744delinsAG
NM_001348946.1:c.2686-1745_2686-1744delinsAG	NP_001335875.1:n.2686-1745_2686-1744delinsAG
NM_001348946.2:c.2686-1745_2686-1744delinsAG MANE Select	NP_001335875.1:n.2686-1745_2686-1744delinsAG
NM_000927.5:c.2686-1745_2686-1744delinsAG	NP_000918.2:n.2686-1745_2686-1744delinsAG
NM_001348944.2:c.2686-1745_2686-1744delinsAG	NP_001335873.1:n.2686-1745_2686-1744delinsAG
NM_001348945.2:c.2896-1745_2896-1744delinsAG	NP_001335874.1:n.2896-1745_2896-1744delinsAG