Canonical Allele Identifier: CA446338197

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131726466A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132390774A>G , CM000667.2:g.132390774A>G	GRCh38
NC_000005.9:g.131726466A>G , CM000667.1:g.131726466A>G	GRCh37
NC_000005.8:g.131754365A>G	NCBI36
NG_008982.1:g.26066A>G
NG_008982.2:g.26071A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.978A>G	ENSP00000388838.2:p.Ser326=
ENST00000435065.7:c.1209A>G	ENSP00000402760.2:p.Ser403=
ENST00000448810.6:c.1053-2A>G	ENSP00000401860.2:n.1053-2A>G
ENST00000685543.1:n.1278A>G
ENST00000686757.1:c.*301A>G	ENSP00000510721.1:n.*301A>G
ENST00000687740.1:n.3822A>G
ENST00000688151.1:n.2447A>G
ENST00000689271.1:c.984A>G	ENSP00000510797.1:p.Ser328=
ENST00000690900.1:c.*301A>G	ENSP00000510703.1:n.*301A>G
ENST00000692212.1:n.2749A>G
ENST00000692355.1:c.390A>G
ENST00000692413.1:c.1119A>G	ENSP00000509374.1:p.Ser373=
ENST00000692825.1:c.1205A>G	ENSP00000509447.1:n.1205A>G
ENST00000693308.1:c.1185A>G	ENSP00000509770.1:p.Ser395=
ENST00000693763.1:n.2297A>G
ENST00000245407.8:c.1137A>G MANE Select	ENSP00000245407.3:p.Ser379=
ENST00000245407.7:c.1137A>G	ENSP00000245407.3:p.Ser379=
ENST00000435065.6:c.1209A>G	ENSP00000402760.2:p.Ser403=
ENST00000447841.5:c.112-1659A>G
ENST00000448810.5:c.401-2A>G
ENST00000461013.5:n.8559A>G
ENST00000475308.1:n.1815A>G
ENST00000479605.5:n.240A>G
NM_001308122.1:c.1209A>G	NP_001295051.1:p.Ser403=
NM_003060.3:c.1137A>G	NP_003051.1:p.Ser379=
XM_011543590.1:c.519A>G	XP_011541892.1:p.Ser173=
XR_427718.1:n.1497A>G
XR_948290.1:n.1394-1659A>G
XR_948291.1:n.1491A>G
XM_011543590.2:c.519A>G	XP_011541892.1:p.Ser173=
XM_017009778.2:c.609A>G	XP_016865267.1:p.Ser203=
XR_001742215.1:n.1394-2A>G
XR_001742216.1:n.1413-2A>G
XR_427718.2:n.1497A>G
XR_948290.2:n.1394-1659A>G
XR_948291.2:n.1491A>G
NM_003060.4:c.1137A>G MANE Select	NP_003051.1:p.Ser379=
NM_001308122.2:c.1209A>G	NP_001295051.1:p.Ser403=