Canonical Allele Identifier: CA342682

Gene: SLC22A5

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132392568C>G , CM000667.2:g.132392568C>G	GRCh38
NC_000005.9:g.131728260C>G , CM000667.1:g.131728260C>G	GRCh37
NC_000005.8:g.131756159C>G	NCBI36
NG_008982.1:g.27860C>G
NG_008982.2:g.27865C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.1244C>G	ENSP00000388838.2:p.Thr415Arg
ENST00000435065.7:c.1475C>G	ENSP00000402760.2:p.Thr492Arg
ENST00000448810.6:c.*255C>G	ENSP00000401860.2:n.*255C>G
ENST00000685543.1:n.1544C>G
ENST00000686757.1:c.*567C>G	ENSP00000510721.1:n.*567C>G
ENST00000687740.1:n.4088C>G
ENST00000688151.1:n.2713C>G
ENST00000689271.1:c.1250C>G	ENSP00000510797.1:p.Thr417Arg
ENST00000690900.1:c.*567C>G	ENSP00000510703.1:n.*567C>G
ENST00000692212.1:n.4543C>G
ENST00000692355.1:c.656C>G
ENST00000692413.1:c.1385C>G	ENSP00000509374.1:p.Thr462Arg
ENST00000692825.1:c.1471C>G	ENSP00000509447.1:n.1471C>G
ENST00000693308.1:c.1451C>G	ENSP00000509770.1:p.Thr484Arg
ENST00000693763.1:n.2563C>G
ENST00000245407.8:c.1403C>G MANE Select	ENSP00000245407.3:p.Thr468Arg
ENST00000245407.7:c.1403C>G	ENSP00000245407.3:p.Thr468Arg
ENST00000435065.6:c.1475C>G	ENSP00000402760.2:p.Thr492Arg
ENST00000447841.5:c.247C>G
ENST00000448810.5:c.665C>G
ENST00000461013.5:n.8825C>G
ENST00000475308.1:n.2081C>G
ENST00000479605.5:n.506C>G
NM_001308122.1:c.1475C>G	NP_001295051.1:p.Thr492Arg
NM_003060.3:c.1403C>G	NP_003051.1:p.Thr468Arg
XM_011543590.1:c.785C>G	XP_011541892.1:p.Thr262Arg
XR_948290.1:n.1529C>G
XM_011543590.2:c.785C>G	XP_011541892.1:p.Thr262Arg
XM_017009778.2:c.875C>G	XP_016865267.1:p.Thr292Arg
XR_001742215.1:n.1658C>G
XR_001742216.1:n.1677C>G
XR_427718.2:n.1763C>G
XR_948290.2:n.1529C>G
XR_948291.2:n.1757C>G
NM_003060.4:c.1403C>G MANE Select	NP_003051.1:p.Thr468Arg
NM_001308122.2:c.1475C>G	NP_001295051.1:p.Thr492Arg