Canonical Allele Identifier: CA1568270787

Gene: SLCO6A1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.102391036A= , CM000667.2:g.102391036A=	GRCh38
NC_000005.9:g.101726740A= , CM000667.1:g.101726740A=	GRCh37
NC_000005.8:g.101754639A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000506729.6:c.1824T= MANE Select	ENSP00000421339.1:p.Pro608=
ENST00000379807.7:c.1824T=	ENSP00000369135.3:p.Pro608=
ENST00000389019.7:c.1638T=	ENSP00000373671.3:p.Pro546=
ENST00000506729.5:c.1824T=	ENSP00000421339.1:p.Pro608=
ENST00000513675.1:c.1065T=	ENSP00000421990.1:p.Pro355=
ENST00000514765.6:n.194T=
NM_001289002.1:c.1824T=	NP_001275931.1:p.Pro608=
NM_001289004.1:c.1638T=	NP_001275933.1:p.Pro546=
NM_001308014.1:c.1065T=	NP_001294943.1:p.Pro355=
NM_173488.4:c.1824T=	NP_775759.3:p.Pro608=
XM_005271874.2:c.1824T=	XP_005271931.1:p.Pro608=
XM_011543147.1:c.1719T=	XP_011541449.1:p.Pro573=
XM_011543148.1:c.1587T=	XP_011541450.1:p.Pro529=
XM_011543149.1:c.1251T=	XP_011541451.1:p.Pro417=
XM_011543150.1:c.1095T=	XP_011541452.1:p.Pro365=
XM_011543151.1:c.1065T=	XP_011541453.1:p.Pro355=
XM_011543153.1:c.1002T=	XP_011541455.1:p.Pro334=
XM_005271874.3:c.1824T=	XP_005271931.1:p.Pro608=
XM_011543147.2:c.1719T=	XP_011541449.1:p.Pro573=
XM_011543148.2:c.1587T=	XP_011541450.1:p.Pro529=
XM_011543153.2:c.1002T=	XP_011541455.1:p.Pro334=
NM_001289002.2:c.1824T=	NP_001275931.1:p.Pro608=
NM_001289004.2:c.1638T=	NP_001275933.1:p.Pro546=
NM_001308014.2:c.1065T=	NP_001294943.1:p.Pro355=
NM_173488.5:c.1824T= MANE Select	NP_775759.3:p.Pro608=