Canonical Allele Identifier: CA2675200009

Gene: SLC22A5

Linked Data

• gnomAD v4: 5-132385310-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132385311del , CM000667.2:g.132385311del	GRCh38
NC_000005.9:g.131721003del , CM000667.1:g.131721003del	GRCh37
NC_000005.8:g.131748902del	NCBI36
NG_008982.1:g.20603del
NG_008982.2:g.20608del

Transcript Alleles

HGVS	Amino-acid change
ENST00000415928.6:c.665+997del	ENSP00000388838.2:n.665+997del
ENST00000435065.7:c.725-17del	ENSP00000402760.2:n.725-17del
ENST00000448810.6:c.653-17del	ENSP00000401860.2:n.653-17del
ENST00000686757.1:c.672-17del	ENSP00000510721.1:n.672-17del
ENST00000687740.1:n.1796del
ENST00000688151.1:n.1845-17del
ENST00000689271.1:c.671+991del	ENSP00000510797.1:n.671+991del
ENST00000690900.1:c.672-65del	ENSP00000510703.1:n.672-65del
ENST00000692212.1:n.462del
ENST00000692355.1:c.204+1010del
ENST00000692413.1:c.672-17del	ENSP00000509374.1:n.672-17del
ENST00000692825.1:c.721-17del	ENSP00000509447.1:n.721-17del
ENST00000693308.1:c.666-17del	ENSP00000509770.1:n.666-17del
ENST00000693763.1:n.1796del
ENST00000245407.8:c.653-17del MANE Select	ENSP00000245407.3:n.653-17del
ENST00000245407.7:c.653-17del	ENSP00000245407.3:n.653-17del
ENST00000415928.5:c.422-17del	ENSP00000388838.1:n.422-17del
ENST00000435065.6:c.725-17del	ENSP00000402760.2:n.725-17del
ENST00000437841.6:c.394-17del	ENSP00000400553.1:n.394-17del
ENST00000461013.5:n.8075-17del
NM_001308122.1:c.725-17del	NP_001295051.1:n.725-17del
NM_003060.3:c.653-17del	NP_003051.1:n.653-17del
XM_011543590.1:c.35-17del	XP_011541892.1:n.35-17del
XR_427718.1:n.1013-17del
XR_948290.1:n.994-17del
XR_948291.1:n.1007-17del
XM_011543590.2:c.35-17del	XP_011541892.1:n.35-17del
XM_017009778.2:c.125-17del	XP_016865267.1:n.125-17del
XR_001742215.1:n.994-17del
XR_001742216.1:n.1013-17del
XR_427718.2:n.1013-17del
XR_948290.2:n.994-17del
XR_948291.2:n.1007-17del
NM_003060.4:c.653-17del MANE Select	NP_003051.1:n.653-17del
NM_001308122.2:c.725-17del	NP_001295051.1:n.725-17del