Canonical Allele Identifier: CA1568270782

Gene: SLCO6A1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.102391017C= , CM000667.2:g.102391017C=	GRCh38
NC_000005.9:g.101726721C= , CM000667.1:g.101726721C=	GRCh37
NC_000005.8:g.101754620C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000506729.6:c.1843G= MANE Select	ENSP00000421339.1:p.Ala615=
ENST00000379807.7:c.1843G=	ENSP00000369135.3:p.Ala615=
ENST00000389019.7:c.1657G=	ENSP00000373671.3:p.Ala553=
ENST00000506729.5:c.1843G=	ENSP00000421339.1:p.Ala615=
ENST00000513675.1:c.1084G=	ENSP00000421990.1:p.Ala362=
ENST00000514765.6:n.213G=
NM_001289002.1:c.1843G=	NP_001275931.1:p.Ala615=
NM_001289004.1:c.1657G=	NP_001275933.1:p.Ala553=
NM_001308014.1:c.1084G=	NP_001294943.1:p.Ala362=
NM_173488.4:c.1843G=	NP_775759.3:p.Ala615=
XM_005271874.2:c.1843G=	XP_005271931.1:p.Ala615=
XM_011543147.1:c.1738G=	XP_011541449.1:p.Ala580=
XM_011543148.1:c.1606G=	XP_011541450.1:p.Ala536=
XM_011543149.1:c.1270G=	XP_011541451.1:p.Ala424=
XM_011543150.1:c.1114G=	XP_011541452.1:p.Ala372=
XM_011543151.1:c.1084G=	XP_011541453.1:p.Ala362=
XM_011543153.1:c.1021G=	XP_011541455.1:p.Ala341=
XM_005271874.3:c.1843G=	XP_005271931.1:p.Ala615=
XM_011543147.2:c.1738G=	XP_011541449.1:p.Ala580=
XM_011543148.2:c.1606G=	XP_011541450.1:p.Ala536=
XM_011543153.2:c.1021G=	XP_011541455.1:p.Ala341=
NM_001289002.2:c.1843G=	NP_001275931.1:p.Ala615=
NM_001289004.2:c.1657G=	NP_001275933.1:p.Ala553=
NM_001308014.2:c.1084G=	NP_001294943.1:p.Ala362=
NM_173488.5:c.1843G= MANE Select	NP_775759.3:p.Ala615=