Canonical Allele Identifier: CA1723631728

Gene: ABCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87530937_87530941delinsAGAAG , CM000669.2:g.87530937_87530941delinsAGAAG	GRCh38
NC_000007.13:g.87160253_87160257delinsAGAAG , CM000669.1:g.87160253_87160257delinsAGAAG	GRCh37
NC_000007.12:g.86998189_86998193delinsAGAAG	NCBI36
NG_011513.1:g.187308_187312delinsCTTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.2685+353_2685+357delinsCTTCT	ENSP00000265724.3:n.2685+353_2685+357delinsCTTCT
ENST00000622132.5:c.2685+353_2685+357delinsCTTCT MANE Select	ENSP00000478255.1:n.2685+353_2685+357delinsCTTCT
ENST00000265724.7:c.2685+353_2685+357delinsCTTCT	ENSP00000265724.3:n.2685+353_2685+357delinsCTTCT
ENST00000488737.6:n.327+353_327+357delinsCTTCT
ENST00000496821.5:n.313+353_313+357delinsCTTCT
ENST00000543898.5:c.2493+353_2493+357delinsCTTCT	ENSP00000444095.1:n.2493+353_2493+357delinsCTTCT
ENST00000622132.4:c.2685+353_2685+357delinsCTTCT	ENSP00000478255.1:n.2685+353_2685+357delinsCTTCT
NM_000927.4:c.2685+353_2685+357delinsCTTCT	NP_000918.2:n.2685+353_2685+357delinsCTTCT
NM_001348944.1:c.2685+353_2685+357delinsCTTCT	NP_001335873.1:n.2685+353_2685+357delinsCTTCT
NM_001348945.1:c.2895+353_2895+357delinsCTTCT	NP_001335874.1:n.2895+353_2895+357delinsCTTCT
NM_001348946.1:c.2685+353_2685+357delinsCTTCT	NP_001335875.1:n.2685+353_2685+357delinsCTTCT
NM_001348946.2:c.2685+353_2685+357delinsCTTCT MANE Select	NP_001335875.1:n.2685+353_2685+357delinsCTTCT
NM_000927.5:c.2685+353_2685+357delinsCTTCT	NP_000918.2:n.2685+353_2685+357delinsCTTCT
NM_001348944.2:c.2685+353_2685+357delinsCTTCT	NP_001335873.1:n.2685+353_2685+357delinsCTTCT
NM_001348945.2:c.2895+353_2895+357delinsCTTCT	NP_001335874.1:n.2895+353_2895+357delinsCTTCT