Canonical Allele Identifier: CA1583144522
Gene: SLC22A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132385297_132385298delinsCT , CM000667.2:g.132385297_132385298delinsCT GRCh38
NC_000005.9:g.131720989_131720990delinsCT , CM000667.1:g.131720989_131720990delinsCT GRCh37
NC_000005.8:g.131748888_131748889delinsCT NCBI36
NG_008982.1:g.20589_20590delinsCT
NG_008982.2:g.20594_20595delinsCT

Transcript Alleles

HGVS Amino-acid change
ENST00000415928.6:c.665+983_665+984delinsCT ENSP00000388838.2:n.665+983_665+984delins...
ENST00000435065.7:c.725-31_725-30delinsCT ENSP00000402760.2:n.725-31_725-30delinsCT...
ENST00000448810.6:c.653-31_653-30delinsCT ENSP00000401860.2:n.653-31_653-30delinsCT...
ENST00000686757.1:c.672-31_672-30delinsCT ENSP00000510721.1:n.672-31_672-30delinsCT...
ENST00000687740.1:n.1782_1783delinsCT
ENST00000688151.1:n.1845-31_1845-30delinsCT
ENST00000689271.1:c.671+977_671+978delinsCT ENSP00000510797.1:n.671+977_671+978delins...
ENST00000690900.1:c.672-79_672-78delinsCT ENSP00000510703.1:n.672-79_672-78delinsCT...
ENST00000692212.1:n.448_449delinsCT
ENST00000692355.1:c.204+996_204+997delinsCT
ENST00000692413.1:c.672-31_672-30delinsCT ENSP00000509374.1:n.672-31_672-30delinsCT...
ENST00000692825.1:c.721-31_721-30delinsCT ENSP00000509447.1:n.721-31_721-30delinsCT...
ENST00000693308.1:c.666-31_666-30delinsCT ENSP00000509770.1:n.666-31_666-30delinsCT...
ENST00000693763.1:n.1782_1783delinsCT
ENST00000245407.8:c.653-31_653-30delinsCT MANE Select ENSP00000245407.3:n.653-31_653-30delinsCT...
ENST00000245407.7:c.653-31_653-30delinsCT ENSP00000245407.3:n.653-31_653-30delinsCT...
ENST00000415928.5:c.422-31_422-30delinsCT ENSP00000388838.1:n.422-31_422-30delinsCT...
ENST00000435065.6:c.725-31_725-30delinsCT ENSP00000402760.2:n.725-31_725-30delinsCT...
ENST00000437841.6:c.394-31_394-30delinsCT ENSP00000400553.1:n.394-31_394-30delinsCT...
ENST00000461013.5:n.8075-31_8075-30delinsCT
NM_001308122.1:c.725-31_725-30delinsCT NP_001295051.1:n.725-31_725-30delinsCT
NM_003060.3:c.653-31_653-30delinsCT NP_003051.1:n.653-31_653-30delinsCT
XM_011543590.1:c.35-31_35-30delinsCT XP_011541892.1:n.35-31_35-30delinsCT
XR_427718.1:n.1013-31_1013-30delinsCT
XR_948290.1:n.994-31_994-30delinsCT
XR_948291.1:n.1007-31_1007-30delinsCT
XM_011543590.2:c.35-31_35-30delinsCT XP_011541892.1:n.35-31_35-30delinsCT
XM_017009778.2:c.125-31_125-30delinsCT XP_016865267.1:n.125-31_125-30delinsCT
XR_001742215.1:n.994-31_994-30delinsCT
XR_001742216.1:n.1013-31_1013-30delinsCT
XR_427718.2:n.1013-31_1013-30delinsCT
XR_948290.2:n.994-31_994-30delinsCT
XR_948291.2:n.1007-31_1007-30delinsCT
NM_003060.4:c.653-31_653-30delinsCT MANE Select NP_003051.1:n.653-31_653-30delinsCT
NM_001308122.2:c.725-31_725-30delinsCT NP_001295051.1:n.725-31_725-30delinsCT