Canonical Allele Identifier: CA6475636

Gene: SLCO1B3 SLCO1B3-SLCO1B7

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.20883557dup , CM000674.2:g.20883557dup	GRCh38
NC_000012.11:g.21036491dup , CM000674.1:g.21036491dup	GRCh37
NC_000012.10:g.20927758dup	NCBI36
NG_032071.1:g.77854dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381545.8:c.1637dup (SLCO1B3) MANE Select	ENSP00000370956.4:p.Leu546PhefsTer21
ENST00000261196.6:c.1637dup (SLCO1B3)	ENSP00000261196.2:p.Leu546PhefsTer21
ENST00000381541.7:c.359+24986dup (SLCO1B3-SLCO1B7)	ENSP00000370952.3:n.359+24986dup
ENST00000381545.7:c.1637dup (SLCO1B3)	ENSP00000370956.3:p.Leu546PhefsTer21
ENST00000540229.1:c.1637dup (SLCO1B3-SLCO1B7)	ENSP00000441269.1:p.Leu546PhefsTer21
ENST00000544370.1:c.1109dup (SLCO1B3)	ENSP00000443225.1:p.Leu370PhefsTer21
NM_019844.3:c.1637dup (SLCO1B3)	NP_062818.1:p.Leu546PhefsTer21
NM_001349920.1:c.1553dup (SLCO1B3)	NP_001336849.1:p.Leu518PhefsTer21
NM_001349920.2:c.1553dup (SLCO1B3)	NP_001336849.1:p.Leu518PhefsTer21
NM_001371097.1:c.1637dup (SLCO1B3-SLCO1B7)	NP_001358026.1:p.Leu546PhefsTer21
NM_019844.4:c.1637dup (SLCO1B3) MANE Select	NP_062818.1:p.Leu546PhefsTer21