Canonical Allele Identifier: CA563057199
Gene: SLC22A5 HGNC NCBI

Linked Data

dbSNP Id: rs1158478659

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132385277A>G , CM000667.2:g.132385277A>G GRCh38
NC_000005.9:g.131720969A>G , CM000667.1:g.131720969A>G GRCh37
NC_000005.8:g.131748868A>G NCBI36
NG_008982.1:g.20569A>G
NG_008982.2:g.20574A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000415928.6:c.665+963A>G ENSP00000388838.2:n.665+963A>G
ENST00000435065.7:c.725-51A>G ENSP00000402760.2:n.725-51A>G
ENST00000448810.6:c.653-51A>G ENSP00000401860.2:n.653-51A>G
ENST00000686757.1:c.672-51A>G ENSP00000510721.1:n.672-51A>G
ENST00000687740.1:n.1762A>G
ENST00000688151.1:n.1845-51A>G
ENST00000689271.1:c.671+957A>G ENSP00000510797.1:n.671+957A>G
ENST00000690900.1:c.672-99A>G ENSP00000510703.1:n.672-99A>G
ENST00000692212.1:n.428A>G
ENST00000692355.1:c.204+976A>G
ENST00000692413.1:c.672-51A>G ENSP00000509374.1:n.672-51A>G
ENST00000692825.1:c.721-51A>G ENSP00000509447.1:n.721-51A>G
ENST00000693308.1:c.666-51A>G ENSP00000509770.1:n.666-51A>G
ENST00000693763.1:n.1762A>G
ENST00000245407.8:c.653-51A>G MANE Select ENSP00000245407.3:n.653-51A>G
ENST00000245407.7:c.653-51A>G ENSP00000245407.3:n.653-51A>G
ENST00000415928.5:c.422-51A>G ENSP00000388838.1:n.422-51A>G
ENST00000435065.6:c.725-51A>G ENSP00000402760.2:n.725-51A>G
ENST00000437841.6:c.394-51A>G ENSP00000400553.1:n.394-51A>G
ENST00000461013.5:n.8075-51A>G
NM_001308122.1:c.725-51A>G NP_001295051.1:n.725-51A>G
NM_003060.3:c.653-51A>G NP_003051.1:n.653-51A>G
XM_011543590.1:c.35-51A>G XP_011541892.1:n.35-51A>G
XR_427718.1:n.1013-51A>G
XR_948290.1:n.994-51A>G
XR_948291.1:n.1007-51A>G
XM_011543590.2:c.35-51A>G XP_011541892.1:n.35-51A>G
XM_017009778.2:c.125-51A>G XP_016865267.1:n.125-51A>G
XR_001742215.1:n.994-51A>G
XR_001742216.1:n.1013-51A>G
XR_427718.2:n.1013-51A>G
XR_948290.2:n.994-51A>G
XR_948291.2:n.1007-51A>G
NM_003060.4:c.653-51A>G MANE Select NP_003051.1:n.653-51A>G
NM_001308122.2:c.725-51A>G NP_001295051.1:n.725-51A>G