Canonical Allele Identifier: CA360807593

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131726461C>G (hg19) ; chr5:g.132390769C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132390769C>G , CM000667.2:g.132390769C>G	GRCh38
NC_000005.9:g.131726461C>G , CM000667.1:g.131726461C>G	GRCh37
NC_000005.8:g.131754360C>G	NCBI36
NG_008982.1:g.26061C>G
NG_008982.2:g.26066C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.973C>G	ENSP00000388838.2:p.Leu325Val
ENST00000435065.7:c.1204C>G	ENSP00000402760.2:p.Leu402Val
ENST00000448810.6:c.1053-7C>G	ENSP00000401860.2:n.1053-7C>G
ENST00000685543.1:n.1273C>G
ENST00000686757.1:c.*296C>G	ENSP00000510721.1:n.*296C>G
ENST00000687740.1:n.3817C>G
ENST00000688151.1:n.2442C>G
ENST00000689271.1:c.979C>G	ENSP00000510797.1:p.Leu327Val
ENST00000690900.1:c.*296C>G	ENSP00000510703.1:n.*296C>G
ENST00000692212.1:n.2744C>G
ENST00000692355.1:c.385C>G
ENST00000692413.1:c.1114C>G	ENSP00000509374.1:p.Leu372Val
ENST00000692825.1:c.1200C>G	ENSP00000509447.1:n.1200C>G
ENST00000693308.1:c.1180C>G	ENSP00000509770.1:p.Leu394Val
ENST00000693763.1:n.2292C>G
ENST00000245407.8:c.1132C>G MANE Select	ENSP00000245407.3:p.Leu378Val
ENST00000245407.7:c.1132C>G	ENSP00000245407.3:p.Leu378Val
ENST00000435065.6:c.1204C>G	ENSP00000402760.2:p.Leu402Val
ENST00000447841.5:c.112-1664C>G
ENST00000448810.5:c.401-7C>G
ENST00000461013.5:n.8554C>G
ENST00000475308.1:n.1810C>G
ENST00000479605.5:n.235C>G
NM_001308122.1:c.1204C>G	NP_001295051.1:p.Leu402Val
NM_003060.3:c.1132C>G	NP_003051.1:p.Leu378Val
XM_011543590.1:c.514C>G	XP_011541892.1:p.Leu172Val
XR_427718.1:n.1492C>G
XR_948290.1:n.1394-1664C>G
XR_948291.1:n.1486C>G
XM_011543590.2:c.514C>G	XP_011541892.1:p.Leu172Val
XM_017009778.2:c.604C>G	XP_016865267.1:p.Leu202Val
XR_001742215.1:n.1394-7C>G
XR_001742216.1:n.1413-7C>G
XR_427718.2:n.1492C>G
XR_948290.2:n.1394-1664C>G
XR_948291.2:n.1486C>G
NM_003060.4:c.1132C>G MANE Select	NP_003051.1:p.Leu378Val
NM_001308122.2:c.1204C>G	NP_001295051.1:p.Leu402Val