Canonical Allele Identifier: CA1583144552
Gene: SLC22A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132393765G= , CM000667.2:g.132393765G= GRCh38
NC_000005.9:g.131729457G= , CM000667.1:g.131729457G= GRCh37
NC_000005.8:g.131757356G= NCBI36
NG_008982.1:g.29057G=
NG_008982.2:g.29062G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000415928.6:c.1292-420G= ENSP00000388838.2:n.1292-420G=
ENST00000435065.7:c.1612G= ENSP00000402760.2:p.Gly538=
ENST00000448810.6:c.*392G= ENSP00000401860.2:n.*392G=
ENST00000685543.1:n.1681G=
ENST00000686757.1:c.*704G= ENSP00000510721.1:n.*704G=
ENST00000686868.1:n.532G=
ENST00000687740.1:n.4225G=
ENST00000688151.1:n.2850G=
ENST00000689271.1:c.1387G= ENSP00000510797.1:p.Gly463=
ENST00000690900.1:c.*704G= ENSP00000510703.1:n.*704G=
ENST00000692212.1:n.4680G=
ENST00000692355.1:c.793G=
ENST00000692413.1:c.1522G= ENSP00000509374.1:p.Gly508=
ENST00000692825.1:c.1608G= ENSP00000509447.1:n.1608G=
ENST00000693308.1:c.1588G= ENSP00000509770.1:p.Gly530=
ENST00000693763.1:n.2700G=
ENST00000245407.8:c.1540G= MANE Select ENSP00000245407.3:p.Gly514=
ENST00000245407.7:c.1540G= ENSP00000245407.3:p.Gly514=
ENST00000435065.6:c.1612G= ENSP00000402760.2:p.Gly538=
ENST00000447841.5:c.384G=
ENST00000448810.5:c.802G=
ENST00000461013.5:n.8962G=
ENST00000475308.1:n.2218G=
NM_001308122.1:c.1612G= NP_001295051.1:p.Gly538=
NM_003060.3:c.1540G= NP_003051.1:p.Gly514=
XM_011543590.1:c.922G= XP_011541892.1:p.Gly308=
XR_948290.1:n.1666G=
XM_011543590.2:c.922G= XP_011541892.1:p.Gly308=
XM_017009778.2:c.1012G= XP_016865267.1:p.Gly338=
XR_001742215.1:n.1795G=
XR_001742216.1:n.1814G=
XR_427718.2:n.1900G=
XR_948290.2:n.1666G=
XR_948291.2:n.1894G=
NM_003060.4:c.1540G= MANE Select NP_003051.1:p.Gly514=
NM_001308122.2:c.1612G= NP_001295051.1:p.Gly538=