Canonical Allele Identifier: CA1568270786

Gene: SLCO6A1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.102391032T= , CM000667.2:g.102391032T=	GRCh38
NC_000005.9:g.101726736T= , CM000667.1:g.101726736T=	GRCh37
NC_000005.8:g.101754635T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000506729.6:c.1828A= MANE Select	ENSP00000421339.1:p.Lys610=
ENST00000379807.7:c.1828A=	ENSP00000369135.3:p.Lys610=
ENST00000389019.7:c.1642A=	ENSP00000373671.3:p.Lys548=
ENST00000506729.5:c.1828A=	ENSP00000421339.1:p.Lys610=
ENST00000513675.1:c.1069A=	ENSP00000421990.1:p.Lys357=
ENST00000514765.6:n.198A=
NM_001289002.1:c.1828A=	NP_001275931.1:p.Lys610=
NM_001289004.1:c.1642A=	NP_001275933.1:p.Lys548=
NM_001308014.1:c.1069A=	NP_001294943.1:p.Lys357=
NM_173488.4:c.1828A=	NP_775759.3:p.Lys610=
XM_005271874.2:c.1828A=	XP_005271931.1:p.Lys610=
XM_011543147.1:c.1723A=	XP_011541449.1:p.Lys575=
XM_011543148.1:c.1591A=	XP_011541450.1:p.Lys531=
XM_011543149.1:c.1255A=	XP_011541451.1:p.Lys419=
XM_011543150.1:c.1099A=	XP_011541452.1:p.Lys367=
XM_011543151.1:c.1069A=	XP_011541453.1:p.Lys357=
XM_011543153.1:c.1006A=	XP_011541455.1:p.Lys336=
XM_005271874.3:c.1828A=	XP_005271931.1:p.Lys610=
XM_011543147.2:c.1723A=	XP_011541449.1:p.Lys575=
XM_011543148.2:c.1591A=	XP_011541450.1:p.Lys531=
XM_011543153.2:c.1006A=	XP_011541455.1:p.Lys336=
NM_001289002.2:c.1828A=	NP_001275931.1:p.Lys610=
NM_001289004.2:c.1642A=	NP_001275933.1:p.Lys548=
NM_001308014.2:c.1069A=	NP_001294943.1:p.Lys357=
NM_173488.5:c.1828A= MANE Select	NP_775759.3:p.Lys610=