Canonical Allele Identifier: CA360573890

Gene: SLCO6A1

Linked Data

• MyVariant Identifiers: chr5:g.101726706A>C (hg19) ; chr5:g.102391002A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.102391002A>C , CM000667.2:g.102391002A>C	GRCh38
NC_000005.9:g.101726706A>C , CM000667.1:g.101726706A>C	GRCh37
NC_000005.8:g.101754605A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000506729.6:c.1858T>G MANE Select	ENSP00000421339.1:p.Tyr620Asp
ENST00000379807.7:c.1858T>G	ENSP00000369135.3:p.Tyr620Asp
ENST00000389019.7:c.1672T>G	ENSP00000373671.3:p.Tyr558Asp
ENST00000506729.5:c.1858T>G	ENSP00000421339.1:p.Tyr620Asp
ENST00000513675.1:c.1099T>G	ENSP00000421990.1:p.Tyr367Asp
ENST00000514765.6:n.228T>G
NM_001289002.1:c.1858T>G	NP_001275931.1:p.Tyr620Asp
NM_001289004.1:c.1672T>G	NP_001275933.1:p.Tyr558Asp
NM_001308014.1:c.1099T>G	NP_001294943.1:p.Tyr367Asp
NM_173488.4:c.1858T>G	NP_775759.3:p.Tyr620Asp
XM_005271874.2:c.1858T>G	XP_005271931.1:p.Tyr620Asp
XM_011543147.1:c.1753T>G	XP_011541449.1:p.Tyr585Asp
XM_011543148.1:c.1621T>G	XP_011541450.1:p.Tyr541Asp
XM_011543149.1:c.1285T>G	XP_011541451.1:p.Tyr429Asp
XM_011543150.1:c.1129T>G	XP_011541452.1:p.Tyr377Asp
XM_011543151.1:c.1099T>G	XP_011541453.1:p.Tyr367Asp
XM_011543153.1:c.1036T>G	XP_011541455.1:p.Tyr346Asp
XM_005271874.3:c.1858T>G	XP_005271931.1:p.Tyr620Asp
XM_011543147.2:c.1753T>G	XP_011541449.1:p.Tyr585Asp
XM_011543148.2:c.1621T>G	XP_011541450.1:p.Tyr541Asp
XM_011543153.2:c.1036T>G	XP_011541455.1:p.Tyr346Asp
NM_001289002.2:c.1858T>G	NP_001275931.1:p.Tyr620Asp
NM_001289004.2:c.1672T>G	NP_001275933.1:p.Tyr558Asp
NM_001308014.2:c.1099T>G	NP_001294943.1:p.Tyr367Asp
NM_173488.5:c.1858T>G MANE Select	NP_775759.3:p.Tyr620Asp