Canonical Allele Identifier: CA445859899

Gene: SLCO6A1

Linked Data

• MyVariant Identifiers: chr5:g.101726689T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.102390985T>G , CM000667.2:g.102390985T>G	GRCh38
NC_000005.9:g.101726689T>G , CM000667.1:g.101726689T>G	GRCh37
NC_000005.8:g.101754588T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000506729.6:c.1875A>C MANE Select	ENSP00000421339.1:p.Ile625=
ENST00000379807.7:c.1875A>C	ENSP00000369135.3:p.Ile625=
ENST00000389019.7:c.1689A>C	ENSP00000373671.3:p.Ile563=
ENST00000506729.5:c.1875A>C	ENSP00000421339.1:p.Ile625=
ENST00000513675.1:c.1116A>C	ENSP00000421990.1:p.Ile372=
ENST00000514765.6:n.245A>C
NM_001289002.1:c.1875A>C	NP_001275931.1:p.Ile625=
NM_001289004.1:c.1689A>C	NP_001275933.1:p.Ile563=
NM_001308014.1:c.1116A>C	NP_001294943.1:p.Ile372=
NM_173488.4:c.1875A>C	NP_775759.3:p.Ile625=
XM_005271874.2:c.1875A>C	XP_005271931.1:p.Ile625=
XM_011543147.1:c.1770A>C	XP_011541449.1:p.Ile590=
XM_011543148.1:c.1638A>C	XP_011541450.1:p.Ile546=
XM_011543149.1:c.1302A>C	XP_011541451.1:p.Ile434=
XM_011543150.1:c.1146A>C	XP_011541452.1:p.Ile382=
XM_011543151.1:c.1116A>C	XP_011541453.1:p.Ile372=
XM_011543153.1:c.1053A>C	XP_011541455.1:p.Ile351=
XM_005271874.3:c.1875A>C	XP_005271931.1:p.Ile625=
XM_011543147.2:c.1770A>C	XP_011541449.1:p.Ile590=
XM_011543148.2:c.1638A>C	XP_011541450.1:p.Ile546=
XM_011543153.2:c.1053A>C	XP_011541455.1:p.Ile351=
NM_001289002.2:c.1875A>C	NP_001275931.1:p.Ile625=
NM_001289004.2:c.1689A>C	NP_001275933.1:p.Ile563=
NM_001308014.2:c.1116A>C	NP_001294943.1:p.Ile372=
NM_173488.5:c.1875A>C MANE Select	NP_775759.3:p.Ile625=