Canonical Allele Identifier: CA1583150021
Gene: SLC22A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132390770T= , CM000667.2:g.132390770T= GRCh38
NC_000005.9:g.131726462T= , CM000667.1:g.131726462T= GRCh37
NC_000005.8:g.131754361T= NCBI36
NG_008982.1:g.26062T=
NG_008982.2:g.26067T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000415928.6:c.974T= ENSP00000388838.2:p.Leu325=
ENST00000435065.7:c.1205T= ENSP00000402760.2:p.Leu402=
ENST00000448810.6:c.1053-6T= ENSP00000401860.2:n.1053-6T=
ENST00000685543.1:n.1274T=
ENST00000686757.1:c.*297T= ENSP00000510721.1:n.*297T=
ENST00000687740.1:n.3818T=
ENST00000688151.1:n.2443T=
ENST00000689271.1:c.980T= ENSP00000510797.1:p.Leu327=
ENST00000690900.1:c.*297T= ENSP00000510703.1:n.*297T=
ENST00000692212.1:n.2745T=
ENST00000692355.1:c.386T=
ENST00000692413.1:c.1115T= ENSP00000509374.1:p.Leu372=
ENST00000692825.1:c.1201T= ENSP00000509447.1:n.1201T=
ENST00000693308.1:c.1181T= ENSP00000509770.1:p.Leu394=
ENST00000693763.1:n.2293T=
ENST00000245407.8:c.1133T= MANE Select ENSP00000245407.3:p.Leu378=
ENST00000245407.7:c.1133T= ENSP00000245407.3:p.Leu378=
ENST00000435065.6:c.1205T= ENSP00000402760.2:p.Leu402=
ENST00000447841.5:c.112-1663T=
ENST00000448810.5:c.401-6T=
ENST00000461013.5:n.8555T=
ENST00000475308.1:n.1811T=
ENST00000479605.5:n.236T=
NM_001308122.1:c.1205T= NP_001295051.1:p.Leu402=
NM_003060.3:c.1133T= NP_003051.1:p.Leu378=
XM_011543590.1:c.515T= XP_011541892.1:p.Leu172=
XR_427718.1:n.1493T=
XR_948290.1:n.1394-1663T=
XR_948291.1:n.1487T=
XM_011543590.2:c.515T= XP_011541892.1:p.Leu172=
XM_017009778.2:c.605T= XP_016865267.1:p.Leu202=
XR_001742215.1:n.1394-6T=
XR_001742216.1:n.1413-6T=
XR_427718.2:n.1493T=
XR_948290.2:n.1394-1663T=
XR_948291.2:n.1487T=
NM_003060.4:c.1133T= MANE Select NP_003051.1:p.Leu378=
NM_001308122.2:c.1205T= NP_001295051.1:p.Leu402=