Canonical Allele Identifier: CA360807502

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131726420A>G (hg19) ; chr5:g.132390728A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132390728A>G , CM000667.2:g.132390728A>G	GRCh38
NC_000005.9:g.131726420A>G , CM000667.1:g.131726420A>G	GRCh37
NC_000005.8:g.131754319A>G	NCBI36
NG_008982.1:g.26020A>G
NG_008982.2:g.26025A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000415928.6:c.932A>G	ENSP00000388838.2:p.Asp311Gly
ENST00000435065.7:c.1163A>G	ENSP00000402760.2:p.Asp388Gly
ENST00000448810.6:c.1053-48A>G	ENSP00000401860.2:n.1053-48A>G
ENST00000685543.1:n.1232A>G
ENST00000686757.1:c.*255A>G	ENSP00000510721.1:n.*255A>G
ENST00000687740.1:n.3776A>G
ENST00000688151.1:n.2401A>G
ENST00000689271.1:c.938A>G	ENSP00000510797.1:p.Asp313Gly
ENST00000690900.1:c.*255A>G	ENSP00000510703.1:n.*255A>G
ENST00000692212.1:n.2703A>G
ENST00000692355.1:c.344A>G
ENST00000692413.1:c.1073A>G	ENSP00000509374.1:p.Asp358Gly
ENST00000692825.1:c.1159A>G	ENSP00000509447.1:n.1159A>G
ENST00000693308.1:c.1139A>G	ENSP00000509770.1:p.Asp380Gly
ENST00000693763.1:n.2251A>G
ENST00000245407.8:c.1091A>G MANE Select	ENSP00000245407.3:p.Asp364Gly
ENST00000245407.7:c.1091A>G	ENSP00000245407.3:p.Asp364Gly
ENST00000435065.6:c.1163A>G	ENSP00000402760.2:p.Asp388Gly
ENST00000447841.5:c.112-1705A>G
ENST00000448810.5:c.401-48A>G
ENST00000461013.5:n.8513A>G
ENST00000475308.1:n.1769A>G
ENST00000479605.5:n.194A>G
NM_001308122.1:c.1163A>G	NP_001295051.1:p.Asp388Gly
NM_003060.3:c.1091A>G	NP_003051.1:p.Asp364Gly
XM_011543590.1:c.473A>G	XP_011541892.1:p.Asp158Gly
XR_427718.1:n.1451A>G
XR_948290.1:n.1394-1705A>G
XR_948291.1:n.1445A>G
XM_011543590.2:c.473A>G	XP_011541892.1:p.Asp158Gly
XM_017009778.2:c.563A>G	XP_016865267.1:p.Asp188Gly
XR_001742215.1:n.1394-48A>G
XR_001742216.1:n.1413-48A>G
XR_427718.2:n.1451A>G
XR_948290.2:n.1394-1705A>G
XR_948291.2:n.1445A>G
NM_003060.4:c.1091A>G MANE Select	NP_003051.1:p.Asp364Gly
NM_001308122.2:c.1163A>G	NP_001295051.1:p.Asp388Gly