Canonical Allele Identifier: CA1081641501

Gene: SLC22A5

Linked Data

• dbSNP Id: rs1752482890
• gnomAD v4: 5-132385275-TAAGG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132385282_132385285del , CM000667.2:g.132385282_132385285del	GRCh38
NC_000005.9:g.131720974_131720977del , CM000667.1:g.131720974_131720977del	GRCh37
NC_000005.8:g.131748873_131748876del	NCBI36
NG_008982.1:g.20574_20577del
NG_008982.2:g.20579_20582del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.665+968_665+971del	ENSP00000388838.2:n.665+968_665+971del
ENST00000435065.7:c.725-46_725-43del	ENSP00000402760.2:n.725-46_725-43del
ENST00000448810.6:c.653-46_653-43del	ENSP00000401860.2:n.653-46_653-43del
ENST00000686757.1:c.672-46_672-43del	ENSP00000510721.1:n.672-46_672-43del
ENST00000687740.1:n.1767_1770del
ENST00000688151.1:n.1845-46_1845-43del
ENST00000689271.1:c.671+962_671+965del	ENSP00000510797.1:n.671+962_671+965del
ENST00000690900.1:c.672-94_672-91del	ENSP00000510703.1:n.672-94_672-91del
ENST00000692212.1:n.433_436del
ENST00000692355.1:c.204+981_204+984del
ENST00000692413.1:c.672-46_672-43del	ENSP00000509374.1:n.672-46_672-43del
ENST00000692825.1:c.721-46_721-43del	ENSP00000509447.1:n.721-46_721-43del
ENST00000693308.1:c.666-46_666-43del	ENSP00000509770.1:n.666-46_666-43del
ENST00000693763.1:n.1767_1770del
ENST00000245407.8:c.653-46_653-43del MANE Select	ENSP00000245407.3:n.653-46_653-43del
ENST00000245407.7:c.653-46_653-43del	ENSP00000245407.3:n.653-46_653-43del
ENST00000415928.5:c.422-46_422-43del	ENSP00000388838.1:n.422-46_422-43del
ENST00000435065.6:c.725-46_725-43del	ENSP00000402760.2:n.725-46_725-43del
ENST00000437841.6:c.394-46_394-43del	ENSP00000400553.1:n.394-46_394-43del
ENST00000461013.5:n.8075-46_8075-43del
NM_001308122.1:c.725-46_725-43del	NP_001295051.1:n.725-46_725-43del
NM_003060.3:c.653-46_653-43del	NP_003051.1:n.653-46_653-43del
XM_011543590.1:c.35-46_35-43del	XP_011541892.1:n.35-46_35-43del
XR_427718.1:n.1013-46_1013-43del
XR_948290.1:n.994-46_994-43del
XR_948291.1:n.1007-46_1007-43del
XM_011543590.2:c.35-46_35-43del	XP_011541892.1:n.35-46_35-43del
XM_017009778.2:c.125-46_125-43del	XP_016865267.1:n.125-46_125-43del
XR_001742215.1:n.994-46_994-43del
XR_001742216.1:n.1013-46_1013-43del
XR_427718.2:n.1013-46_1013-43del
XR_948290.2:n.994-46_994-43del
XR_948291.2:n.1007-46_1007-43del
NM_003060.4:c.653-46_653-43del MANE Select	NP_003051.1:n.653-46_653-43del
NM_001308122.2:c.725-46_725-43del	NP_001295051.1:n.725-46_725-43del