Canonical Allele Identifier: CA1723630881

Gene: ABCB1

Linked Data

• dbSNP Id: rs1816000847

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87530789_87530790insCAAGAAAG , CM000669.2:g.87530789_87530790insCAAGAAAG	GRCh38
NC_000007.13:g.87160105_87160106insCAAGAAAG , CM000669.1:g.87160105_87160106insCAAGAAAG	GRCh37
NC_000007.12:g.86998041_86998042insCAAGAAAG	NCBI36
NG_011513.1:g.187463_187464insCTTGCTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.2685+508_2685+509insCTTGCTTT	ENSP00000265724.3:n.2685+508_2685+509insCTTGCTTT
ENST00000622132.5:c.2685+508_2685+509insCTTGCTTT MANE Select	ENSP00000478255.1:n.2685+508_2685+509insCTTGCTTT
ENST00000265724.7:c.2685+508_2685+509insCTTGCTTT	ENSP00000265724.3:n.2685+508_2685+509insCTTGCTTT
ENST00000488737.6:n.327+508_327+509insCTTGCTTT
ENST00000496821.5:n.313+508_313+509insCTTGCTTT
ENST00000543898.5:c.2493+508_2493+509insCTTGCTTT	ENSP00000444095.1:n.2493+508_2493+509insCTTGCTTT
ENST00000622132.4:c.2685+508_2685+509insCTTGCTTT	ENSP00000478255.1:n.2685+508_2685+509insCTTGCTTT
NM_000927.4:c.2685+508_2685+509insCTTGCTTT	NP_000918.2:n.2685+508_2685+509insCTTGCTTT
NM_001348944.1:c.2685+508_2685+509insCTTGCTTT	NP_001335873.1:n.2685+508_2685+509insCTTGCTTT
NM_001348945.1:c.2895+508_2895+509insCTTGCTTT	NP_001335874.1:n.2895+508_2895+509insCTTGCTTT
NM_001348946.1:c.2685+508_2685+509insCTTGCTTT	NP_001335875.1:n.2685+508_2685+509insCTTGCTTT
NM_001348946.2:c.2685+508_2685+509insCTTGCTTT MANE Select	NP_001335875.1:n.2685+508_2685+509insCTTGCTTT
NM_000927.5:c.2685+508_2685+509insCTTGCTTT	NP_000918.2:n.2685+508_2685+509insCTTGCTTT
NM_001348944.2:c.2685+508_2685+509insCTTGCTTT	NP_001335873.1:n.2685+508_2685+509insCTTGCTTT
NM_001348945.2:c.2895+508_2895+509insCTTGCTTT	NP_001335874.1:n.2895+508_2895+509insCTTGCTTT