Canonical Allele Identifier: CA1583144581
Gene: SLC22A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132393787T= , CM000667.2:g.132393787T= GRCh38
NC_000005.9:g.131729479T= , CM000667.1:g.131729479T= GRCh37
NC_000005.8:g.131757378T= NCBI36
NG_008982.1:g.29079T=
NG_008982.2:g.29084T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000415928.6:c.1292-398T= ENSP00000388838.2:n.1292-398T=
ENST00000435065.7:c.1634T= ENSP00000402760.2:p.Ile545=
ENST00000448810.6:c.*414T= ENSP00000401860.2:n.*414T=
ENST00000685543.1:n.1703T=
ENST00000686757.1:c.*726T= ENSP00000510721.1:n.*726T=
ENST00000686868.1:n.554T=
ENST00000687740.1:n.4247T=
ENST00000688151.1:n.2872T=
ENST00000689271.1:c.1409T= ENSP00000510797.1:p.Ile470=
ENST00000690900.1:c.*726T= ENSP00000510703.1:n.*726T=
ENST00000692212.1:n.4702T=
ENST00000692355.1:c.815T=
ENST00000692413.1:c.1544T= ENSP00000509374.1:p.Ile515=
ENST00000692825.1:c.1630T= ENSP00000509447.1:n.1630T=
ENST00000693308.1:c.1610T= ENSP00000509770.1:p.Ile537=
ENST00000693763.1:n.2722T=
ENST00000245407.8:c.1562T= MANE Select ENSP00000245407.3:p.Ile521=
ENST00000245407.7:c.1562T= ENSP00000245407.3:p.Ile521=
ENST00000435065.6:c.1634T= ENSP00000402760.2:p.Ile545=
ENST00000447841.5:c.406T=
ENST00000448810.5:c.824T=
ENST00000461013.5:n.8984T=
ENST00000475308.1:n.2240T=
NM_001308122.1:c.1634T= NP_001295051.1:p.Ile545=
NM_003060.3:c.1562T= NP_003051.1:p.Ile521=
XM_011543590.1:c.944T= XP_011541892.1:p.Ile315=
XR_948290.1:n.1688T=
XM_011543590.2:c.944T= XP_011541892.1:p.Ile315=
XM_017009778.2:c.1034T= XP_016865267.1:p.Ile345=
XR_001742215.1:n.1817T=
XR_001742216.1:n.1836T=
XR_427718.2:n.1922T=
XR_948290.2:n.1688T=
XR_948291.2:n.1916T=
NM_003060.4:c.1562T= MANE Select NP_003051.1:p.Ile521=
NM_001308122.2:c.1634T= NP_001295051.1:p.Ile545=