Canonical Allele Identifier: CA1583144394
Gene: SLC22A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132393676G= , CM000667.2:g.132393676G= GRCh38
NC_000005.9:g.131729368G= , CM000667.1:g.131729368G= GRCh37
NC_000005.8:g.131757267G= NCBI36
NG_008982.1:g.28968G=
NG_008982.2:g.28973G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000415928.6:c.1292-509G= ENSP00000388838.2:n.1292-509G=
ENST00000435065.7:c.1523G= ENSP00000402760.2:p.Gly508=
ENST00000448810.6:c.*303G= ENSP00000401860.2:n.*303G=
ENST00000685543.1:n.1592G=
ENST00000686757.1:c.*615G= ENSP00000510721.1:n.*615G=
ENST00000686868.1:n.443G=
ENST00000687740.1:n.4136G=
ENST00000688151.1:n.2761G=
ENST00000689271.1:c.1298G= ENSP00000510797.1:p.Gly433=
ENST00000690900.1:c.*615G= ENSP00000510703.1:n.*615G=
ENST00000692212.1:n.4591G=
ENST00000692355.1:c.704G=
ENST00000692413.1:c.1433G= ENSP00000509374.1:p.Gly478=
ENST00000692825.1:c.1519G= ENSP00000509447.1:n.1519G=
ENST00000693308.1:c.1499G= ENSP00000509770.1:p.Gly500=
ENST00000693763.1:n.2611G=
ENST00000245407.8:c.1451G= MANE Select ENSP00000245407.3:p.Gly484=
ENST00000245407.7:c.1451G= ENSP00000245407.3:p.Gly484=
ENST00000435065.6:c.1523G= ENSP00000402760.2:p.Gly508=
ENST00000447841.5:c.295G=
ENST00000448810.5:c.713G=
ENST00000461013.5:n.8873G=
ENST00000475308.1:n.2129G=
ENST00000479605.5:n.554G=
NM_001308122.1:c.1523G= NP_001295051.1:p.Gly508=
NM_003060.3:c.1451G= NP_003051.1:p.Gly484=
XM_011543590.1:c.833G= XP_011541892.1:p.Gly278=
XR_948290.1:n.1577G=
XM_011543590.2:c.833G= XP_011541892.1:p.Gly278=
XM_017009778.2:c.923G= XP_016865267.1:p.Gly308=
XR_001742215.1:n.1706G=
XR_001742216.1:n.1725G=
XR_427718.2:n.1811G=
XR_948290.2:n.1577G=
XR_948291.2:n.1805G=
NM_003060.4:c.1451G= MANE Select NP_003051.1:p.Gly484=
NM_001308122.2:c.1523G= NP_001295051.1:p.Gly508=