Canonical Allele Identifier: CA2675199934

Gene: SLC22A5

Linked Data

• gnomAD v4: 5-132385220-A-ACT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132385220_132385221insCT , CM000667.2:g.132385220_132385221insCT	GRCh38
NC_000005.9:g.131720912_131720913insCT , CM000667.1:g.131720912_131720913insCT	GRCh37
NC_000005.8:g.131748811_131748812insCT	NCBI36
NG_008982.1:g.20512_20513insCT
NG_008982.2:g.20517_20518insCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000415928.6:c.665+906_665+907insCT	ENSP00000388838.2:n.665+906_665+907insCT
ENST00000435065.7:c.725-108_725-107insCT	ENSP00000402760.2:n.725-108_725-107insCT
ENST00000448810.6:c.653-108_653-107insCT	ENSP00000401860.2:n.653-108_653-107insCT
ENST00000686757.1:c.672-108_672-107insCT	ENSP00000510721.1:n.672-108_672-107insCT
ENST00000687740.1:n.1705_1706insCT
ENST00000688151.1:n.1845-108_1845-107insCT
ENST00000689271.1:c.671+900_671+901insCT	ENSP00000510797.1:n.671+900_671+901insCT
ENST00000690900.1:c.672-156_672-155insCT	ENSP00000510703.1:n.672-156_672-155insCT
ENST00000692212.1:n.371_372insCT
ENST00000692355.1:c.204+919_204+920insCT
ENST00000692413.1:c.672-108_672-107insCT	ENSP00000509374.1:n.672-108_672-107insCT
ENST00000692825.1:c.721-108_721-107insCT	ENSP00000509447.1:n.721-108_721-107insCT
ENST00000693308.1:c.666-108_666-107insCT	ENSP00000509770.1:n.666-108_666-107insCT
ENST00000693763.1:n.1705_1706insCT
ENST00000245407.8:c.653-108_653-107insCT MANE Select	ENSP00000245407.3:n.653-108_653-107insCT
ENST00000245407.7:c.653-108_653-107insCT	ENSP00000245407.3:n.653-108_653-107insCT
ENST00000415928.5:c.422-108_422-107insCT	ENSP00000388838.1:n.422-108_422-107insCT
ENST00000435065.6:c.725-108_725-107insCT	ENSP00000402760.2:n.725-108_725-107insCT
ENST00000437841.6:c.394-108_394-107insCT	ENSP00000400553.1:n.394-108_394-107insCT
ENST00000461013.5:n.8075-108_8075-107insCT
NM_001308122.1:c.725-108_725-107insCT	NP_001295051.1:n.725-108_725-107insCT
NM_003060.3:c.653-108_653-107insCT	NP_003051.1:n.653-108_653-107insCT
XM_011543590.1:c.35-108_35-107insCT	XP_011541892.1:n.35-108_35-107insCT
XR_427718.1:n.1013-108_1013-107insCT
XR_948290.1:n.994-108_994-107insCT
XR_948291.1:n.1007-108_1007-107insCT
XM_011543590.2:c.35-108_35-107insCT	XP_011541892.1:n.35-108_35-107insCT
XM_017009778.2:c.125-108_125-107insCT	XP_016865267.1:n.125-108_125-107insCT
XR_001742215.1:n.994-108_994-107insCT
XR_001742216.1:n.1013-108_1013-107insCT
XR_427718.2:n.1013-108_1013-107insCT
XR_948290.2:n.994-108_994-107insCT
XR_948291.2:n.1007-108_1007-107insCT
NM_003060.4:c.653-108_653-107insCT MANE Select	NP_003051.1:n.653-108_653-107insCT
NM_001308122.2:c.725-108_725-107insCT	NP_001295051.1:n.725-108_725-107insCT