Canonical Allele Identifier: CA1583144504

Gene: SLC22A5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132385242_132385244delinsCTG , CM000667.2:g.132385242_132385244delinsCTG	GRCh38
NC_000005.9:g.131720934_131720936delinsCTG , CM000667.1:g.131720934_131720936delinsCTG	GRCh37
NC_000005.8:g.131748833_131748835delinsCTG	NCBI36
NG_008982.1:g.20534_20536delinsCTG
NG_008982.2:g.20539_20541delinsCTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000415928.6:c.665+928_665+930delinsCTG	ENSP00000388838.2:n.665+928_665+930delinsCTG
ENST00000435065.7:c.725-86_725-84delinsCTG	ENSP00000402760.2:n.725-86_725-84delinsCTG
ENST00000448810.6:c.653-86_653-84delinsCTG	ENSP00000401860.2:n.653-86_653-84delinsCTG
ENST00000686757.1:c.672-86_672-84delinsCTG	ENSP00000510721.1:n.672-86_672-84delinsCTG
ENST00000687740.1:n.1727_1729delinsCTG
ENST00000688151.1:n.1845-86_1845-84delinsCTG
ENST00000689271.1:c.671+922_671+924delinsCTG	ENSP00000510797.1:n.671+922_671+924delinsCTG
ENST00000690900.1:c.672-134_672-132delinsCTG	ENSP00000510703.1:n.672-134_672-132delinsCTG
ENST00000692212.1:n.393_395delinsCTG
ENST00000692355.1:c.204+941_204+943delinsCTG
ENST00000692413.1:c.672-86_672-84delinsCTG	ENSP00000509374.1:n.672-86_672-84delinsCTG
ENST00000692825.1:c.721-86_721-84delinsCTG	ENSP00000509447.1:n.721-86_721-84delinsCTG
ENST00000693308.1:c.666-86_666-84delinsCTG	ENSP00000509770.1:n.666-86_666-84delinsCTG
ENST00000693763.1:n.1727_1729delinsCTG
ENST00000245407.8:c.653-86_653-84delinsCTG MANE Select	ENSP00000245407.3:n.653-86_653-84delinsCTG
ENST00000245407.7:c.653-86_653-84delinsCTG	ENSP00000245407.3:n.653-86_653-84delinsCTG
ENST00000415928.5:c.422-86_422-84delinsCTG	ENSP00000388838.1:n.422-86_422-84delinsCTG
ENST00000435065.6:c.725-86_725-84delinsCTG	ENSP00000402760.2:n.725-86_725-84delinsCTG
ENST00000437841.6:c.394-86_394-84delinsCTG	ENSP00000400553.1:n.394-86_394-84delinsCTG
ENST00000461013.5:n.8075-86_8075-84delinsCTG
NM_001308122.1:c.725-86_725-84delinsCTG	NP_001295051.1:n.725-86_725-84delinsCTG
NM_003060.3:c.653-86_653-84delinsCTG	NP_003051.1:n.653-86_653-84delinsCTG
XM_011543590.1:c.35-86_35-84delinsCTG	XP_011541892.1:n.35-86_35-84delinsCTG
XR_427718.1:n.1013-86_1013-84delinsCTG
XR_948290.1:n.994-86_994-84delinsCTG
XR_948291.1:n.1007-86_1007-84delinsCTG
XM_011543590.2:c.35-86_35-84delinsCTG	XP_011541892.1:n.35-86_35-84delinsCTG
XM_017009778.2:c.125-86_125-84delinsCTG	XP_016865267.1:n.125-86_125-84delinsCTG
XR_001742215.1:n.994-86_994-84delinsCTG
XR_001742216.1:n.1013-86_1013-84delinsCTG
XR_427718.2:n.1013-86_1013-84delinsCTG
XR_948290.2:n.994-86_994-84delinsCTG
XR_948291.2:n.1007-86_1007-84delinsCTG
NM_003060.4:c.653-86_653-84delinsCTG MANE Select	NP_003051.1:n.653-86_653-84delinsCTG
NM_001308122.2:c.725-86_725-84delinsCTG	NP_001295051.1:n.725-86_725-84delinsCTG