Canonical Allele Identifier: CA445859897

Gene: SLCO6A1

Linked Data

• MyVariant Identifiers: chr5:g.101726686A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.102390982A>G , CM000667.2:g.102390982A>G	GRCh38
NC_000005.9:g.101726686A>G , CM000667.1:g.101726686A>G	GRCh37
NC_000005.8:g.101754585A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000506729.6:c.1878T>C MANE Select	ENSP00000421339.1:p.Phe626=
ENST00000379807.7:c.1878T>C	ENSP00000369135.3:p.Phe626=
ENST00000389019.7:c.1692T>C	ENSP00000373671.3:p.Phe564=
ENST00000506729.5:c.1878T>C	ENSP00000421339.1:p.Phe626=
ENST00000513675.1:c.1119T>C	ENSP00000421990.1:p.Phe373=
ENST00000514765.6:n.248T>C
NM_001289002.1:c.1878T>C	NP_001275931.1:p.Phe626=
NM_001289004.1:c.1692T>C	NP_001275933.1:p.Phe564=
NM_001308014.1:c.1119T>C	NP_001294943.1:p.Phe373=
NM_173488.4:c.1878T>C	NP_775759.3:p.Phe626=
XM_005271874.2:c.1878T>C	XP_005271931.1:p.Phe626=
XM_011543147.1:c.1773T>C	XP_011541449.1:p.Phe591=
XM_011543148.1:c.1641T>C	XP_011541450.1:p.Phe547=
XM_011543149.1:c.1305T>C	XP_011541451.1:p.Phe435=
XM_011543150.1:c.1149T>C	XP_011541452.1:p.Phe383=
XM_011543151.1:c.1119T>C	XP_011541453.1:p.Phe373=
XM_011543153.1:c.1056T>C	XP_011541455.1:p.Phe352=
XM_005271874.3:c.1878T>C	XP_005271931.1:p.Phe626=
XM_011543147.2:c.1773T>C	XP_011541449.1:p.Phe591=
XM_011543148.2:c.1641T>C	XP_011541450.1:p.Phe547=
XM_011543153.2:c.1056T>C	XP_011541455.1:p.Phe352=
NM_001289002.2:c.1878T>C	NP_001275931.1:p.Phe626=
NM_001289004.2:c.1692T>C	NP_001275933.1:p.Phe564=
NM_001308014.2:c.1119T>C	NP_001294943.1:p.Phe373=
NM_173488.5:c.1878T>C MANE Select	NP_775759.3:p.Phe626=