Canonical Allele Identifier: CA446339613

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131726535C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132390843C>G , CM000667.2:g.132390843C>G	GRCh38
NC_000005.9:g.131726535C>G , CM000667.1:g.131726535C>G	GRCh37
NC_000005.8:g.131754434C>G	NCBI36
NG_008982.1:g.26135C>G
NG_008982.2:g.26140C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.1047C>G	ENSP00000388838.2:p.Ser349=
ENST00000435065.7:c.1278C>G	ENSP00000402760.2:p.Ser426=
ENST00000448810.6:c.*58C>G	ENSP00000401860.2:n.*58C>G
ENST00000685543.1:n.1347C>G
ENST00000686757.1:c.*370C>G	ENSP00000510721.1:n.*370C>G
ENST00000687740.1:n.3891C>G
ENST00000688151.1:n.2516C>G
ENST00000689271.1:c.1053C>G	ENSP00000510797.1:p.Ser351=
ENST00000690900.1:c.*370C>G	ENSP00000510703.1:n.*370C>G
ENST00000692212.1:n.2818C>G
ENST00000692355.1:c.459C>G
ENST00000692413.1:c.1188C>G	ENSP00000509374.1:p.Ser396=
ENST00000692825.1:c.1274C>G	ENSP00000509447.1:n.1274C>G
ENST00000693308.1:c.1254C>G	ENSP00000509770.1:p.Ser418=
ENST00000693763.1:n.2366C>G
ENST00000245407.8:c.1206C>G MANE Select	ENSP00000245407.3:p.Ser402=
ENST00000245407.7:c.1206C>G	ENSP00000245407.3:p.Ser402=
ENST00000435065.6:c.1278C>G	ENSP00000402760.2:p.Ser426=
ENST00000447841.5:c.112-1590C>G
ENST00000448810.5:c.468C>G
ENST00000461013.5:n.8628C>G
ENST00000475308.1:n.1884C>G
ENST00000479605.5:n.309C>G
NM_001308122.1:c.1278C>G	NP_001295051.1:p.Ser426=
NM_003060.3:c.1206C>G	NP_003051.1:p.Ser402=
XM_011543590.1:c.588C>G	XP_011541892.1:p.Ser196=
XR_427718.1:n.1566C>G
XR_948290.1:n.1394-1590C>G
XR_948291.1:n.1560C>G
XM_011543590.2:c.588C>G	XP_011541892.1:p.Ser196=
XM_017009778.2:c.678C>G	XP_016865267.1:p.Ser226=
XR_001742215.1:n.1461C>G
XR_001742216.1:n.1480C>G
XR_427718.2:n.1566C>G
XR_948290.2:n.1394-1590C>G
XR_948291.2:n.1560C>G
NM_003060.4:c.1206C>G MANE Select	NP_003051.1:p.Ser402=
NM_001308122.2:c.1278C>G	NP_001295051.1:p.Ser426=