Canonical Allele Identifier: CA2020829491

Gene: SLCO1B3 SLCO1B3-SLCO1B7

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.20892815_20892816delinsCT , CM000674.2:g.20892815_20892816delinsCT	GRCh38
NC_000012.11:g.21045749_21045750delinsCT , CM000674.1:g.21045749_21045750delinsCT	GRCh37
NC_000012.10:g.20937016_20937017delinsCT	NCBI36
NG_032071.1:g.87112_87113delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000381545.8:c.1683-5621_1683-5620delinsCT (SLCO1B3) MANE Select	ENSP00000370956.4:n.1683-5621_1683-5620de...
ENST00000261196.6:c.1683-5621_1683-5620delinsCT (SLCO1B3)	ENSP00000261196.2:n.1683-5621_1683-5620de...
ENST00000381541.7:c.359+34244_359+34245delinsCT (SLCO1B3-SLCO1B7)	ENSP00000370952.3:n.359+34244_359+34245de...
ENST00000381545.7:c.1683-5621_1683-5620delinsCT (SLCO1B3)	ENSP00000370956.3:n.1683-5621_1683-5620de...
ENST00000540229.1:c.1683-5621_1683-5620delinsCT (SLCO1B3-SLCO1B7)	ENSP00000441269.1:n.1683-5621_1683-5620de...
ENST00000544370.1:c.1155-5621_1155-5620delinsCT (SLCO1B3)	ENSP00000443225.1:n.1155-5621_1155-5620de...
NM_019844.3:c.1683-5621_1683-5620delinsCT (SLCO1B3)	NP_062818.1:n.1683-5621_1683-5620delinsCT...
NM_001349920.1:c.1599-5621_1599-5620delinsCT (SLCO1B3)	NP_001336849.1:n.1599-5621_1599-5620delin...
NM_001349920.2:c.1599-5621_1599-5620delinsCT (SLCO1B3)	NP_001336849.1:n.1599-5621_1599-5620delin...
NM_001371097.1:c.1683-5621_1683-5620delinsCT (SLCO1B3-SLCO1B7)	NP_001358026.1:n.1683-5621_1683-5620delin...
NM_019844.4:c.1683-5621_1683-5620delinsCT (SLCO1B3) MANE Select	NP_062818.1:n.1683-5621_1683-5620delinsCT...