Canonical Allele Identifier: CA446339928

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131726562C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132390870C>G , CM000667.2:g.132390870C>G	GRCh38
NC_000005.9:g.131726562C>G , CM000667.1:g.131726562C>G	GRCh37
NC_000005.8:g.131754461C>G	NCBI36
NG_008982.1:g.26162C>G
NG_008982.2:g.26167C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.1074C>G	ENSP00000388838.2:p.Gly358=
ENST00000435065.7:c.1305C>G	ENSP00000402760.2:p.Gly435=
ENST00000448810.6:c.*85C>G	ENSP00000401860.2:n.*85C>G
ENST00000685543.1:n.1374C>G
ENST00000686757.1:c.*397C>G	ENSP00000510721.1:n.*397C>G
ENST00000687740.1:n.3918C>G
ENST00000688151.1:n.2543C>G
ENST00000689271.1:c.1080C>G	ENSP00000510797.1:p.Gly360=
ENST00000690900.1:c.*397C>G	ENSP00000510703.1:n.*397C>G
ENST00000692212.1:n.2845C>G
ENST00000692355.1:c.486C>G
ENST00000692413.1:c.1215C>G	ENSP00000509374.1:p.Gly405=
ENST00000692825.1:c.1301C>G	ENSP00000509447.1:n.1301C>G
ENST00000693308.1:c.1281C>G	ENSP00000509770.1:p.Gly427=
ENST00000693763.1:n.2393C>G
ENST00000245407.8:c.1233C>G MANE Select	ENSP00000245407.3:p.Gly411=
ENST00000245407.7:c.1233C>G	ENSP00000245407.3:p.Gly411=
ENST00000435065.6:c.1305C>G	ENSP00000402760.2:p.Gly435=
ENST00000447841.5:c.112-1563C>G
ENST00000448810.5:c.495C>G
ENST00000461013.5:n.8655C>G
ENST00000475308.1:n.1911C>G
ENST00000479605.5:n.336C>G
NM_001308122.1:c.1305C>G	NP_001295051.1:p.Gly435=
NM_003060.3:c.1233C>G	NP_003051.1:p.Gly411=
XM_011543590.1:c.615C>G	XP_011541892.1:p.Gly205=
XR_427718.1:n.1593C>G
XR_948290.1:n.1394-1563C>G
XR_948291.1:n.1587C>G
XM_011543590.2:c.615C>G	XP_011541892.1:p.Gly205=
XM_017009778.2:c.705C>G	XP_016865267.1:p.Gly235=
XR_001742215.1:n.1488C>G
XR_001742216.1:n.1507C>G
XR_427718.2:n.1593C>G
XR_948290.2:n.1394-1563C>G
XR_948291.2:n.1587C>G
NM_003060.4:c.1233C>G MANE Select	NP_003051.1:p.Gly411=
NM_001308122.2:c.1305C>G	NP_001295051.1:p.Gly435=