Canonical Allele Identifier: CA1583150286
Gene: SLC22A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132390889C= , CM000667.2:g.132390889C= GRCh38
NC_000005.9:g.131726581C= , CM000667.1:g.131726581C= GRCh37
NC_000005.8:g.131754480C= NCBI36
NG_008982.1:g.26181C=
NG_008982.2:g.26186C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000415928.6:c.1093C= ENSP00000388838.2:p.Gln365=
ENST00000435065.7:c.1324C= ENSP00000402760.2:p.Gln442=
ENST00000448810.6:c.*104C= ENSP00000401860.2:n.*104C=
ENST00000685543.1:n.1393C=
ENST00000686757.1:c.*416C= ENSP00000510721.1:n.*416C=
ENST00000687740.1:n.3937C=
ENST00000688151.1:n.2562C=
ENST00000689271.1:c.1099C= ENSP00000510797.1:p.Gln367=
ENST00000690900.1:c.*416C= ENSP00000510703.1:n.*416C=
ENST00000692212.1:n.2864C=
ENST00000692355.1:c.505C=
ENST00000692413.1:c.1234C= ENSP00000509374.1:p.Gln412=
ENST00000692825.1:c.1320C= ENSP00000509447.1:n.1320C=
ENST00000693308.1:c.1300C= ENSP00000509770.1:p.Gln434=
ENST00000693763.1:n.2412C=
ENST00000245407.8:c.1252C= MANE Select ENSP00000245407.3:p.Gln418=
ENST00000245407.7:c.1252C= ENSP00000245407.3:p.Gln418=
ENST00000435065.6:c.1324C= ENSP00000402760.2:p.Gln442=
ENST00000447841.5:c.112-1544C=
ENST00000448810.5:c.514C=
ENST00000461013.5:n.8674C=
ENST00000475308.1:n.1930C=
ENST00000479605.5:n.355C=
NM_001308122.1:c.1324C= NP_001295051.1:p.Gln442=
NM_003060.3:c.1252C= NP_003051.1:p.Gln418=
XM_011543590.1:c.634C= XP_011541892.1:p.Gln212=
XR_427718.1:n.1612C=
XR_948290.1:n.1394-1544C=
XR_948291.1:n.1606C=
XM_011543590.2:c.634C= XP_011541892.1:p.Gln212=
XM_017009778.2:c.724C= XP_016865267.1:p.Gln242=
XR_001742215.1:n.1507C=
XR_001742216.1:n.1526C=
XR_427718.2:n.1612C=
XR_948290.2:n.1394-1544C=
XR_948291.2:n.1606C=
NM_003060.4:c.1252C= MANE Select NP_003051.1:p.Gln418=
NM_001308122.2:c.1324C= NP_001295051.1:p.Gln442=