Canonical Allele Identifier: CA360809891

Gene: SLC22A5

Linked Data

• dbSNP Id: rs1580895879
• MyVariant Identifiers: chr5:g.131729452G>A (hg19) ; chr5:g.132393760G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132393760G>A , CM000667.2:g.132393760G>A	GRCh38
NC_000005.9:g.131729452G>A , CM000667.1:g.131729452G>A	GRCh37
NC_000005.8:g.131757351G>A	NCBI36
NG_008982.1:g.29052G>A
NG_008982.2:g.29057G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.1292-425G>A	ENSP00000388838.2:n.1292-425G>A
ENST00000435065.7:c.1607G>A	ENSP00000402760.2:p.Ser536Asn
ENST00000448810.6:c.*387G>A	ENSP00000401860.2:n.*387G>A
ENST00000685543.1:n.1676G>A
ENST00000686757.1:c.*699G>A	ENSP00000510721.1:n.*699G>A
ENST00000686868.1:n.527G>A
ENST00000687740.1:n.4220G>A
ENST00000688151.1:n.2845G>A
ENST00000689271.1:c.1382G>A	ENSP00000510797.1:p.Ser461Asn
ENST00000690900.1:c.*699G>A	ENSP00000510703.1:n.*699G>A
ENST00000692212.1:n.4675G>A
ENST00000692355.1:c.788G>A
ENST00000692413.1:c.1517G>A	ENSP00000509374.1:p.Ser506Asn
ENST00000692825.1:c.1603G>A	ENSP00000509447.1:n.1603G>A
ENST00000693308.1:c.1583G>A	ENSP00000509770.1:p.Ser528Asn
ENST00000693763.1:n.2695G>A
ENST00000245407.8:c.1535G>A MANE Select	ENSP00000245407.3:p.Ser512Asn
ENST00000245407.7:c.1535G>A	ENSP00000245407.3:p.Ser512Asn
ENST00000435065.6:c.1607G>A	ENSP00000402760.2:p.Ser536Asn
ENST00000447841.5:c.379G>A
ENST00000448810.5:c.797G>A
ENST00000461013.5:n.8957G>A
ENST00000475308.1:n.2213G>A
NM_001308122.1:c.1607G>A	NP_001295051.1:p.Ser536Asn
NM_003060.3:c.1535G>A	NP_003051.1:p.Ser512Asn
XM_011543590.1:c.917G>A	XP_011541892.1:p.Ser306Asn
XR_948290.1:n.1661G>A
XM_011543590.2:c.917G>A	XP_011541892.1:p.Ser306Asn
XM_017009778.2:c.1007G>A	XP_016865267.1:p.Ser336Asn
XR_001742215.1:n.1790G>A
XR_001742216.1:n.1809G>A
XR_427718.2:n.1895G>A
XR_948290.2:n.1661G>A
XR_948291.2:n.1889G>A
NM_003060.4:c.1535G>A MANE Select	NP_003051.1:p.Ser512Asn
NM_001308122.2:c.1607G>A	NP_001295051.1:p.Ser536Asn