Canonical Allele Identifier: CA360805508

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131722721A>G (hg19) ; chr5:g.132387029A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132387029A>G , CM000667.2:g.132387029A>G	GRCh38
NC_000005.9:g.131722721A>G , CM000667.1:g.131722721A>G	GRCh37
NC_000005.8:g.131750620A>G	NCBI36
NG_008982.1:g.22321A>G
NG_008982.2:g.22326A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.670A>G	ENSP00000388838.2:p.Ile224Val
ENST00000435065.7:c.901A>G	ENSP00000402760.2:p.Ile301Val
ENST00000448810.6:c.829A>G	ENSP00000401860.2:p.Ile277Val
ENST00000686757.1:c.848A>G	ENSP00000510721.1:p.His283Arg
ENST00000687740.1:n.3514A>G
ENST00000688151.1:n.2139A>G
ENST00000689271.1:c.676A>G	ENSP00000510797.1:p.Ile226Val
ENST00000690900.1:c.800A>G	ENSP00000510703.1:p.His267Arg
ENST00000692212.1:n.773A>G
ENST00000692355.1:c.205-1892A>G
ENST00000692413.1:c.844-33A>G	ENSP00000509374.1:n.844-33A>G
ENST00000692825.1:c.897A>G	ENSP00000509447.1:n.897A>G
ENST00000693308.1:c.877A>G	ENSP00000509770.1:p.Ile293Val
ENST00000693763.1:n.1989A>G
ENST00000245407.8:c.829A>G MANE Select	ENSP00000245407.3:p.Ile277Val
ENST00000245407.7:c.829A>G	ENSP00000245407.3:p.Ile277Val
ENST00000415928.5:c.598A>G	ENSP00000388838.1:p.Ile200Val
ENST00000435065.6:c.901A>G	ENSP00000402760.2:p.Ile301Val
ENST00000437841.6:c.*144A>G	ENSP00000400553.1:n.*144A>G
ENST00000448810.5:c.177A>G
ENST00000461013.5:n.8251A>G
NM_001308122.1:c.901A>G	NP_001295051.1:p.Ile301Val
NM_003060.3:c.829A>G	NP_003051.1:p.Ile277Val
XM_011543590.1:c.211A>G	XP_011541892.1:p.Ile71Val
XR_427718.1:n.1189A>G
XR_948290.1:n.1170A>G
XR_948291.1:n.1183A>G
XM_011543590.2:c.211A>G	XP_011541892.1:p.Ile71Val
XM_017009778.2:c.301A>G	XP_016865267.1:p.Ile101Val
XR_001742215.1:n.1170A>G
XR_001742216.1:n.1189A>G
XR_427718.2:n.1189A>G
XR_948290.2:n.1170A>G
XR_948291.2:n.1183A>G
NM_003060.4:c.829A>G MANE Select	NP_003051.1:p.Ile277Val
NM_001308122.2:c.901A>G	NP_001295051.1:p.Ile301Val