Canonical Allele Identifier: CA360807625

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131726477A>G (hg19) ; chr5:g.132390785A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132390785A>G , CM000667.2:g.132390785A>G	GRCh38
NC_000005.9:g.131726477A>G , CM000667.1:g.131726477A>G	GRCh37
NC_000005.8:g.131754376A>G	NCBI36
NG_008982.1:g.26077A>G
NG_008982.2:g.26082A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.989A>G	ENSP00000388838.2:p.Glu330Gly
ENST00000435065.7:c.1220A>G	ENSP00000402760.2:p.Glu407Gly
ENST00000448810.6:c.1062A>G	ENSP00000401860.2:p.Ter354Trp
ENST00000685543.1:n.1289A>G
ENST00000686757.1:c.*312A>G	ENSP00000510721.1:n.*312A>G
ENST00000687740.1:n.3833A>G
ENST00000688151.1:n.2458A>G
ENST00000689271.1:c.995A>G	ENSP00000510797.1:p.Glu332Gly
ENST00000690900.1:c.*312A>G	ENSP00000510703.1:n.*312A>G
ENST00000692212.1:n.2760A>G
ENST00000692355.1:c.401A>G
ENST00000692413.1:c.1130A>G	ENSP00000509374.1:p.Glu377Gly
ENST00000692825.1:c.1216A>G	ENSP00000509447.1:n.1216A>G
ENST00000693308.1:c.1196A>G	ENSP00000509770.1:p.Glu399Gly
ENST00000693763.1:n.2308A>G
ENST00000245407.8:c.1148A>G MANE Select	ENSP00000245407.3:p.Glu383Gly
ENST00000245407.7:c.1148A>G	ENSP00000245407.3:p.Glu383Gly
ENST00000435065.6:c.1220A>G	ENSP00000402760.2:p.Glu407Gly
ENST00000447841.5:c.112-1648A>G
ENST00000448810.5:c.410A>G
ENST00000461013.5:n.8570A>G
ENST00000475308.1:n.1826A>G
ENST00000479605.5:n.251A>G
NM_001308122.1:c.1220A>G	NP_001295051.1:p.Glu407Gly
NM_003060.3:c.1148A>G	NP_003051.1:p.Glu383Gly
XM_011543590.1:c.530A>G	XP_011541892.1:p.Glu177Gly
XR_427718.1:n.1508A>G
XR_948290.1:n.1394-1648A>G
XR_948291.1:n.1502A>G
XM_011543590.2:c.530A>G	XP_011541892.1:p.Glu177Gly
XM_017009778.2:c.620A>G	XP_016865267.1:p.Glu207Gly
XR_001742215.1:n.1403A>G
XR_001742216.1:n.1422A>G
XR_427718.2:n.1508A>G
XR_948290.2:n.1394-1648A>G
XR_948291.2:n.1502A>G
NM_003060.4:c.1148A>G MANE Select	NP_003051.1:p.Glu383Gly
NM_001308122.2:c.1220A>G	NP_001295051.1:p.Glu407Gly