Canonical Allele Identifier: CA127209228

Gene: SLC22A5

Linked Data

• dbSNP Id: rs1041320507
• MyVariant Identifiers: chr5:g.131720935_131720936del (hg19) ; chr5:g.132385243_132385244del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132385246_132385247del , CM000667.2:g.132385246_132385247del	GRCh38
NC_000005.9:g.131720938_131720939del , CM000667.1:g.131720938_131720939del	GRCh37
NC_000005.8:g.131748837_131748838del	NCBI36
NG_008982.1:g.20538_20539del
NG_008982.2:g.20543_20544del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.665+932_665+933del	ENSP00000388838.2:n.665+932_665+933del
ENST00000435065.7:c.725-82_725-81del	ENSP00000402760.2:n.725-82_725-81del
ENST00000448810.6:c.653-82_653-81del	ENSP00000401860.2:n.653-82_653-81del
ENST00000686757.1:c.672-82_672-81del	ENSP00000510721.1:n.672-82_672-81del
ENST00000687740.1:n.1731_1732del
ENST00000688151.1:n.1845-82_1845-81del
ENST00000689271.1:c.671+926_671+927del	ENSP00000510797.1:n.671+926_671+927del
ENST00000690900.1:c.672-130_672-129del	ENSP00000510703.1:n.672-130_672-129del
ENST00000692212.1:n.397_398del
ENST00000692355.1:c.204+945_204+946del
ENST00000692413.1:c.672-82_672-81del	ENSP00000509374.1:n.672-82_672-81del
ENST00000692825.1:c.721-82_721-81del	ENSP00000509447.1:n.721-82_721-81del
ENST00000693308.1:c.666-82_666-81del	ENSP00000509770.1:n.666-82_666-81del
ENST00000693763.1:n.1731_1732del
ENST00000245407.8:c.653-82_653-81del MANE Select	ENSP00000245407.3:n.653-82_653-81del
ENST00000245407.7:c.653-82_653-81del	ENSP00000245407.3:n.653-82_653-81del
ENST00000415928.5:c.422-82_422-81del	ENSP00000388838.1:n.422-82_422-81del
ENST00000435065.6:c.725-82_725-81del	ENSP00000402760.2:n.725-82_725-81del
ENST00000437841.6:c.394-82_394-81del	ENSP00000400553.1:n.394-82_394-81del
ENST00000461013.5:n.8075-82_8075-81del
NM_001308122.1:c.725-82_725-81del	NP_001295051.1:n.725-82_725-81del
NM_003060.3:c.653-82_653-81del	NP_003051.1:n.653-82_653-81del
XM_011543590.1:c.35-82_35-81del	XP_011541892.1:n.35-82_35-81del
XR_427718.1:n.1013-82_1013-81del
XR_948290.1:n.994-82_994-81del
XR_948291.1:n.1007-82_1007-81del
XM_011543590.2:c.35-82_35-81del	XP_011541892.1:n.35-82_35-81del
XM_017009778.2:c.125-82_125-81del	XP_016865267.1:n.125-82_125-81del
XR_001742215.1:n.994-82_994-81del
XR_001742216.1:n.1013-82_1013-81del
XR_427718.2:n.1013-82_1013-81del
XR_948290.2:n.994-82_994-81del
XR_948291.2:n.1007-82_1007-81del
NM_003060.4:c.653-82_653-81del MANE Select	NP_003051.1:n.653-82_653-81del
NM_001308122.2:c.725-82_725-81del	NP_001295051.1:n.725-82_725-81del