Canonical Allele Identifier: CA360807735

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131726531A>G (hg19) ; chr5:g.132390839A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132390839A>G , CM000667.2:g.132390839A>G	GRCh38
NC_000005.9:g.131726531A>G , CM000667.1:g.131726531A>G	GRCh37
NC_000005.8:g.131754430A>G	NCBI36
NG_008982.1:g.26131A>G
NG_008982.2:g.26136A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.1043A>G	ENSP00000388838.2:p.Tyr348Cys
ENST00000435065.7:c.1274A>G	ENSP00000402760.2:p.Tyr425Cys
ENST00000448810.6:c.*54A>G	ENSP00000401860.2:n.*54A>G
ENST00000685543.1:n.1343A>G
ENST00000686757.1:c.*366A>G	ENSP00000510721.1:n.*366A>G
ENST00000687740.1:n.3887A>G
ENST00000688151.1:n.2512A>G
ENST00000689271.1:c.1049A>G	ENSP00000510797.1:p.Tyr350Cys
ENST00000690900.1:c.*366A>G	ENSP00000510703.1:n.*366A>G
ENST00000692212.1:n.2814A>G
ENST00000692355.1:c.455A>G
ENST00000692413.1:c.1184A>G	ENSP00000509374.1:p.Tyr395Cys
ENST00000692825.1:c.1270A>G	ENSP00000509447.1:n.1270A>G
ENST00000693308.1:c.1250A>G	ENSP00000509770.1:p.Tyr417Cys
ENST00000693763.1:n.2362A>G
ENST00000245407.8:c.1202A>G MANE Select	ENSP00000245407.3:p.Tyr401Cys
ENST00000245407.7:c.1202A>G	ENSP00000245407.3:p.Tyr401Cys
ENST00000435065.6:c.1274A>G	ENSP00000402760.2:p.Tyr425Cys
ENST00000447841.5:c.112-1594A>G
ENST00000448810.5:c.464A>G
ENST00000461013.5:n.8624A>G
ENST00000475308.1:n.1880A>G
ENST00000479605.5:n.305A>G
NM_001308122.1:c.1274A>G	NP_001295051.1:p.Tyr425Cys
NM_003060.3:c.1202A>G	NP_003051.1:p.Tyr401Cys
XM_011543590.1:c.584A>G	XP_011541892.1:p.Tyr195Cys
XR_427718.1:n.1562A>G
XR_948290.1:n.1394-1594A>G
XR_948291.1:n.1556A>G
XM_011543590.2:c.584A>G	XP_011541892.1:p.Tyr195Cys
XM_017009778.2:c.674A>G	XP_016865267.1:p.Tyr225Cys
XR_001742215.1:n.1457A>G
XR_001742216.1:n.1476A>G
XR_427718.2:n.1562A>G
XR_948290.2:n.1394-1594A>G
XR_948291.2:n.1556A>G
NM_003060.4:c.1202A>G MANE Select	NP_003051.1:p.Tyr401Cys
NM_001308122.2:c.1274A>G	NP_001295051.1:p.Tyr425Cys