Canonical Allele Identifier: CA1583150303
Gene: SLC22A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132390899C= , CM000667.2:g.132390899C= GRCh38
NC_000005.9:g.131726591C= , CM000667.1:g.131726591C= GRCh37
NC_000005.8:g.131754490C= NCBI36
NG_008982.1:g.26191C=
NG_008982.2:g.26196C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000415928.6:c.1103C= ENSP00000388838.2:p.Pro368=
ENST00000435065.7:c.1334C= ENSP00000402760.2:p.Pro445=
ENST00000448810.6:c.*114C= ENSP00000401860.2:n.*114C=
ENST00000685543.1:n.1403C=
ENST00000686757.1:c.*426C= ENSP00000510721.1:n.*426C=
ENST00000687740.1:n.3947C=
ENST00000688151.1:n.2572C=
ENST00000689271.1:c.1109C= ENSP00000510797.1:p.Pro370=
ENST00000690900.1:c.*426C= ENSP00000510703.1:n.*426C=
ENST00000692212.1:n.2874C=
ENST00000692355.1:c.515C=
ENST00000692413.1:c.1244C= ENSP00000509374.1:p.Pro415=
ENST00000692825.1:c.1330C= ENSP00000509447.1:n.1330C=
ENST00000693308.1:c.1310C= ENSP00000509770.1:p.Pro437=
ENST00000693763.1:n.2422C=
ENST00000245407.8:c.1262C= MANE Select ENSP00000245407.3:p.Pro421=
ENST00000245407.7:c.1262C= ENSP00000245407.3:p.Pro421=
ENST00000435065.6:c.1334C= ENSP00000402760.2:p.Pro445=
ENST00000447841.5:c.112-1534C=
ENST00000448810.5:c.524C=
ENST00000461013.5:n.8684C=
ENST00000475308.1:n.1940C=
ENST00000479605.5:n.365C=
NM_001308122.1:c.1334C= NP_001295051.1:p.Pro445=
NM_003060.3:c.1262C= NP_003051.1:p.Pro421=
XM_011543590.1:c.644C= XP_011541892.1:p.Pro215=
XR_427718.1:n.1622C=
XR_948290.1:n.1394-1534C=
XR_948291.1:n.1616C=
XM_011543590.2:c.644C= XP_011541892.1:p.Pro215=
XM_017009778.2:c.734C= XP_016865267.1:p.Pro245=
XR_001742215.1:n.1517C=
XR_001742216.1:n.1536C=
XR_427718.2:n.1622C=
XR_948290.2:n.1394-1534C=
XR_948291.2:n.1616C=
NM_003060.4:c.1262C= MANE Select NP_003051.1:p.Pro421=
NM_001308122.2:c.1334C= NP_001295051.1:p.Pro445=