Canonical Allele Identifier: CA445859907

Gene: SLCO6A1

Linked Data

• MyVariant Identifiers: chr5:g.101726701C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.102390997C>G , CM000667.2:g.102390997C>G	GRCh38
NC_000005.9:g.101726701C>G , CM000667.1:g.101726701C>G	GRCh37
NC_000005.8:g.101754600C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000506729.6:c.1863G>C MANE Select	ENSP00000421339.1:p.Val621=
ENST00000379807.7:c.1863G>C	ENSP00000369135.3:p.Val621=
ENST00000389019.7:c.1677G>C	ENSP00000373671.3:p.Val559=
ENST00000506729.5:c.1863G>C	ENSP00000421339.1:p.Val621=
ENST00000513675.1:c.1104G>C	ENSP00000421990.1:p.Val368=
ENST00000514765.6:n.233G>C
NM_001289002.1:c.1863G>C	NP_001275931.1:p.Val621=
NM_001289004.1:c.1677G>C	NP_001275933.1:p.Val559=
NM_001308014.1:c.1104G>C	NP_001294943.1:p.Val368=
NM_173488.4:c.1863G>C	NP_775759.3:p.Val621=
XM_005271874.2:c.1863G>C	XP_005271931.1:p.Val621=
XM_011543147.1:c.1758G>C	XP_011541449.1:p.Val586=
XM_011543148.1:c.1626G>C	XP_011541450.1:p.Val542=
XM_011543149.1:c.1290G>C	XP_011541451.1:p.Val430=
XM_011543150.1:c.1134G>C	XP_011541452.1:p.Val378=
XM_011543151.1:c.1104G>C	XP_011541453.1:p.Val368=
XM_011543153.1:c.1041G>C	XP_011541455.1:p.Val347=
XM_005271874.3:c.1863G>C	XP_005271931.1:p.Val621=
XM_011543147.2:c.1758G>C	XP_011541449.1:p.Val586=
XM_011543148.2:c.1626G>C	XP_011541450.1:p.Val542=
XM_011543153.2:c.1041G>C	XP_011541455.1:p.Val347=
NM_001289002.2:c.1863G>C	NP_001275931.1:p.Val621=
NM_001289004.2:c.1677G>C	NP_001275933.1:p.Val559=
NM_001308014.2:c.1104G>C	NP_001294943.1:p.Val368=
NM_173488.5:c.1863G>C MANE Select	NP_775759.3:p.Val621=