Canonical Allele Identifier: CA1568270790
Gene: SLCO6A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.102391040A= , CM000667.2:g.102391040A= GRCh38
NC_000005.9:g.101726744A= , CM000667.1:g.101726744A= GRCh37
NC_000005.8:g.101754643A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000506729.6:c.1820T= MANE Select ENSP00000421339.1:p.Val607=
ENST00000379807.7:c.1820T= ENSP00000369135.3:p.Val607=
ENST00000389019.7:c.1634T= ENSP00000373671.3:p.Val545=
ENST00000506729.5:c.1820T= ENSP00000421339.1:p.Val607=
ENST00000513675.1:c.1061T= ENSP00000421990.1:p.Val354=
ENST00000514765.6:n.190T=
NM_001289002.1:c.1820T= NP_001275931.1:p.Val607=
NM_001289004.1:c.1634T= NP_001275933.1:p.Val545=
NM_001308014.1:c.1061T= NP_001294943.1:p.Val354=
NM_173488.4:c.1820T= NP_775759.3:p.Val607=
XM_005271874.2:c.1820T= XP_005271931.1:p.Val607=
XM_011543147.1:c.1715T= XP_011541449.1:p.Val572=
XM_011543148.1:c.1583T= XP_011541450.1:p.Val528=
XM_011543149.1:c.1247T= XP_011541451.1:p.Val416=
XM_011543150.1:c.1091T= XP_011541452.1:p.Val364=
XM_011543151.1:c.1061T= XP_011541453.1:p.Val354=
XM_011543153.1:c.998T= XP_011541455.1:p.Val333=
XM_005271874.3:c.1820T= XP_005271931.1:p.Val607=
XM_011543147.2:c.1715T= XP_011541449.1:p.Val572=
XM_011543148.2:c.1583T= XP_011541450.1:p.Val528=
XM_011543153.2:c.998T= XP_011541455.1:p.Val333=
NM_001289002.2:c.1820T= NP_001275931.1:p.Val607=
NM_001289004.2:c.1634T= NP_001275933.1:p.Val545=
NM_001308014.2:c.1061T= NP_001294943.1:p.Val354=
NM_173488.5:c.1820T= MANE Select NP_775759.3:p.Val607=