Canonical Allele Identifier: CA360809564

Gene: SLC22A5

Linked Data

• dbSNP Id: rs1447092948
• MyVariant Identifiers: chr5:g.131729371C>G (hg19) ; chr5:g.132393679C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132393679C>G , CM000667.2:g.132393679C>G	GRCh38
NC_000005.9:g.131729371C>G , CM000667.1:g.131729371C>G	GRCh37
NC_000005.8:g.131757270C>G	NCBI36
NG_008982.1:g.28971C>G
NG_008982.2:g.28976C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.1292-506C>G	ENSP00000388838.2:n.1292-506C>G
ENST00000435065.7:c.1526C>G	ENSP00000402760.2:p.Ala509Gly
ENST00000448810.6:c.*306C>G	ENSP00000401860.2:n.*306C>G
ENST00000685543.1:n.1595C>G
ENST00000686757.1:c.*618C>G	ENSP00000510721.1:n.*618C>G
ENST00000686868.1:n.446C>G
ENST00000687740.1:n.4139C>G
ENST00000688151.1:n.2764C>G
ENST00000689271.1:c.1301C>G	ENSP00000510797.1:p.Ala434Gly
ENST00000690900.1:c.*618C>G	ENSP00000510703.1:n.*618C>G
ENST00000692212.1:n.4594C>G
ENST00000692355.1:c.707C>G
ENST00000692413.1:c.1436C>G	ENSP00000509374.1:p.Ala479Gly
ENST00000692825.1:c.1522C>G	ENSP00000509447.1:n.1522C>G
ENST00000693308.1:c.1502C>G	ENSP00000509770.1:p.Ala501Gly
ENST00000693763.1:n.2614C>G
ENST00000245407.8:c.1454C>G MANE Select	ENSP00000245407.3:p.Ala485Gly
ENST00000245407.7:c.1454C>G	ENSP00000245407.3:p.Ala485Gly
ENST00000435065.6:c.1526C>G	ENSP00000402760.2:p.Ala509Gly
ENST00000447841.5:c.298C>G
ENST00000448810.5:c.716C>G
ENST00000461013.5:n.8876C>G
ENST00000475308.1:n.2132C>G
ENST00000479605.5:n.557C>G
NM_001308122.1:c.1526C>G	NP_001295051.1:p.Ala509Gly
NM_003060.3:c.1454C>G	NP_003051.1:p.Ala485Gly
XM_011543590.1:c.836C>G	XP_011541892.1:p.Ala279Gly
XR_948290.1:n.1580C>G
XM_011543590.2:c.836C>G	XP_011541892.1:p.Ala279Gly
XM_017009778.2:c.926C>G	XP_016865267.1:p.Ala309Gly
XR_001742215.1:n.1709C>G
XR_001742216.1:n.1728C>G
XR_427718.2:n.1814C>G
XR_948290.2:n.1580C>G
XR_948291.2:n.1808C>G
NM_003060.4:c.1454C>G MANE Select	NP_003051.1:p.Ala485Gly
NM_001308122.2:c.1526C>G	NP_001295051.1:p.Ala509Gly