Canonical Allele Identifier: CA360810038

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131729493A>G (hg19) ; chr5:g.132393801A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132393801A>G , CM000667.2:g.132393801A>G	GRCh38
NC_000005.9:g.131729493A>G , CM000667.1:g.131729493A>G	GRCh37
NC_000005.8:g.131757392A>G	NCBI36
NG_008982.1:g.29093A>G
NG_008982.2:g.29098A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.1292-384A>G	ENSP00000388838.2:n.1292-384A>G
ENST00000435065.7:c.1648A>G	ENSP00000402760.2:p.Arg550Gly
ENST00000448810.6:c.*428A>G	ENSP00000401860.2:n.*428A>G
ENST00000685543.1:n.1717A>G
ENST00000686757.1:c.*740A>G	ENSP00000510721.1:n.*740A>G
ENST00000686868.1:n.568A>G
ENST00000687740.1:n.4261A>G
ENST00000688151.1:n.2886A>G
ENST00000689271.1:c.1423A>G	ENSP00000510797.1:p.Arg475Gly
ENST00000690900.1:c.*740A>G	ENSP00000510703.1:n.*740A>G
ENST00000692212.1:n.4716A>G
ENST00000692355.1:c.829A>G
ENST00000692413.1:c.1558A>G	ENSP00000509374.1:p.Arg520Gly
ENST00000692825.1:c.1644A>G	ENSP00000509447.1:n.1644A>G
ENST00000693308.1:c.1624A>G	ENSP00000509770.1:p.Arg542Gly
ENST00000693763.1:n.2736A>G
ENST00000245407.8:c.1576A>G MANE Select	ENSP00000245407.3:p.Arg526Gly
ENST00000245407.7:c.1576A>G	ENSP00000245407.3:p.Arg526Gly
ENST00000435065.6:c.1648A>G	ENSP00000402760.2:p.Arg550Gly
ENST00000447841.5:c.420A>G
ENST00000448810.5:c.838A>G
ENST00000461013.5:n.8998A>G
ENST00000475308.1:n.2254A>G
NM_001308122.1:c.1648A>G	NP_001295051.1:p.Arg550Gly
NM_003060.3:c.1576A>G	NP_003051.1:p.Arg526Gly
XM_011543590.1:c.958A>G	XP_011541892.1:p.Arg320Gly
XR_948290.1:n.1702A>G
XM_011543590.2:c.958A>G	XP_011541892.1:p.Arg320Gly
XM_017009778.2:c.1048A>G	XP_016865267.1:p.Arg350Gly
XR_001742215.1:n.1831A>G
XR_001742216.1:n.1850A>G
XR_427718.2:n.1936A>G
XR_948290.2:n.1702A>G
XR_948291.2:n.1930A>G
NM_003060.4:c.1576A>G MANE Select	NP_003051.1:p.Arg526Gly
NM_001308122.2:c.1648A>G	NP_001295051.1:p.Arg550Gly