Canonical Allele Identifier: CA360573960

Gene: SLCO6A1

Linked Data

• MyVariant Identifiers: chr5:g.101726723A>G (hg19) ; chr5:g.102391019A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.102391019A>G , CM000667.2:g.102391019A>G	GRCh38
NC_000005.9:g.101726723A>G , CM000667.1:g.101726723A>G	GRCh37
NC_000005.8:g.101754622A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000506729.6:c.1841T>C MANE Select	ENSP00000421339.1:p.Leu614Pro
ENST00000379807.7:c.1841T>C	ENSP00000369135.3:p.Leu614Pro
ENST00000389019.7:c.1655T>C	ENSP00000373671.3:p.Leu552Pro
ENST00000506729.5:c.1841T>C	ENSP00000421339.1:p.Leu614Pro
ENST00000513675.1:c.1082T>C	ENSP00000421990.1:p.Leu361Pro
ENST00000514765.6:n.211T>C
NM_001289002.1:c.1841T>C	NP_001275931.1:p.Leu614Pro
NM_001289004.1:c.1655T>C	NP_001275933.1:p.Leu552Pro
NM_001308014.1:c.1082T>C	NP_001294943.1:p.Leu361Pro
NM_173488.4:c.1841T>C	NP_775759.3:p.Leu614Pro
XM_005271874.2:c.1841T>C	XP_005271931.1:p.Leu614Pro
XM_011543147.1:c.1736T>C	XP_011541449.1:p.Leu579Pro
XM_011543148.1:c.1604T>C	XP_011541450.1:p.Leu535Pro
XM_011543149.1:c.1268T>C	XP_011541451.1:p.Leu423Pro
XM_011543150.1:c.1112T>C	XP_011541452.1:p.Leu371Pro
XM_011543151.1:c.1082T>C	XP_011541453.1:p.Leu361Pro
XM_011543153.1:c.1019T>C	XP_011541455.1:p.Leu340Pro
XM_005271874.3:c.1841T>C	XP_005271931.1:p.Leu614Pro
XM_011543147.2:c.1736T>C	XP_011541449.1:p.Leu579Pro
XM_011543148.2:c.1604T>C	XP_011541450.1:p.Leu535Pro
XM_011543153.2:c.1019T>C	XP_011541455.1:p.Leu340Pro
NM_001289002.2:c.1841T>C	NP_001275931.1:p.Leu614Pro
NM_001289004.2:c.1655T>C	NP_001275933.1:p.Leu552Pro
NM_001308014.2:c.1082T>C	NP_001294943.1:p.Leu361Pro
NM_173488.5:c.1841T>C MANE Select	NP_775759.3:p.Leu614Pro