Canonical Allele Identifier: CA360807707

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131726516A>G (hg19) ; chr5:g.132390824A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132390824A>G , CM000667.2:g.132390824A>G	GRCh38
NC_000005.9:g.131726516A>G , CM000667.1:g.131726516A>G	GRCh37
NC_000005.8:g.131754415A>G	NCBI36
NG_008982.1:g.26116A>G
NG_008982.2:g.26121A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000415928.6:c.1028A>G	ENSP00000388838.2:p.Tyr343Cys
ENST00000435065.7:c.1259A>G	ENSP00000402760.2:p.Tyr420Cys
ENST00000448810.6:c.*39A>G	ENSP00000401860.2:n.*39A>G
ENST00000685543.1:n.1328A>G
ENST00000686757.1:c.*351A>G	ENSP00000510721.1:n.*351A>G
ENST00000687740.1:n.3872A>G
ENST00000688151.1:n.2497A>G
ENST00000689271.1:c.1034A>G	ENSP00000510797.1:p.Tyr345Cys
ENST00000690900.1:c.*351A>G	ENSP00000510703.1:n.*351A>G
ENST00000692212.1:n.2799A>G
ENST00000692355.1:c.440A>G
ENST00000692413.1:c.1169A>G	ENSP00000509374.1:p.Tyr390Cys
ENST00000692825.1:c.1255A>G	ENSP00000509447.1:n.1255A>G
ENST00000693308.1:c.1235A>G	ENSP00000509770.1:p.Tyr412Cys
ENST00000693763.1:n.2347A>G
ENST00000245407.8:c.1187A>G MANE Select	ENSP00000245407.3:p.Tyr396Cys
ENST00000245407.7:c.1187A>G	ENSP00000245407.3:p.Tyr396Cys
ENST00000435065.6:c.1259A>G	ENSP00000402760.2:p.Tyr420Cys
ENST00000447841.5:c.112-1609A>G
ENST00000448810.5:c.449A>G
ENST00000461013.5:n.8609A>G
ENST00000475308.1:n.1865A>G
ENST00000479605.5:n.290A>G
NM_001308122.1:c.1259A>G	NP_001295051.1:p.Tyr420Cys
NM_003060.3:c.1187A>G	NP_003051.1:p.Tyr396Cys
XM_011543590.1:c.569A>G	XP_011541892.1:p.Tyr190Cys
XR_427718.1:n.1547A>G
XR_948290.1:n.1394-1609A>G
XR_948291.1:n.1541A>G
XM_011543590.2:c.569A>G	XP_011541892.1:p.Tyr190Cys
XM_017009778.2:c.659A>G	XP_016865267.1:p.Tyr220Cys
XR_001742215.1:n.1442A>G
XR_001742216.1:n.1461A>G
XR_427718.2:n.1547A>G
XR_948290.2:n.1394-1609A>G
XR_948291.2:n.1541A>G
NM_003060.4:c.1187A>G MANE Select	NP_003051.1:p.Tyr396Cys
NM_001308122.2:c.1259A>G	NP_001295051.1:p.Tyr420Cys