Canonical Allele Identifier: CA1583144376

Gene: SLC22A5

Linked Data

• dbSNP Id: rs1752472483

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132384964T>G , CM000667.2:g.132384964T>G	GRCh38
NC_000005.9:g.131720656T>G , CM000667.1:g.131720656T>G	GRCh37
NC_000005.8:g.131748555T>G	NCBI36
NG_008982.1:g.20256T>G
NG_008982.2:g.20261T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.665+650T>G	ENSP00000388838.2:n.665+650T>G
ENST00000435065.7:c.725-364T>G	ENSP00000402760.2:n.725-364T>G
ENST00000448810.6:c.653-364T>G	ENSP00000401860.2:n.653-364T>G
ENST00000686757.1:c.672-364T>G	ENSP00000510721.1:n.672-364T>G
ENST00000687740.1:n.1449T>G
ENST00000688151.1:n.1845-364T>G
ENST00000689271.1:c.671+644T>G	ENSP00000510797.1:n.671+644T>G
ENST00000690900.1:c.672-412T>G	ENSP00000510703.1:n.672-412T>G
ENST00000692212.1:n.115T>G
ENST00000692355.1:c.204+663T>G
ENST00000692413.1:c.672-364T>G	ENSP00000509374.1:n.672-364T>G
ENST00000692825.1:c.721-364T>G	ENSP00000509447.1:n.721-364T>G
ENST00000693308.1:c.666-364T>G	ENSP00000509770.1:n.666-364T>G
ENST00000693763.1:n.1449T>G
ENST00000245407.8:c.653-364T>G MANE Select	ENSP00000245407.3:n.653-364T>G
ENST00000245407.7:c.653-364T>G	ENSP00000245407.3:n.653-364T>G
ENST00000415928.5:c.422-364T>G	ENSP00000388838.1:n.422-364T>G
ENST00000435065.6:c.725-364T>G	ENSP00000402760.2:n.725-364T>G
ENST00000437841.6:c.394-364T>G	ENSP00000400553.1:n.394-364T>G
ENST00000461013.5:n.8075-364T>G
NM_001308122.1:c.725-364T>G	NP_001295051.1:n.725-364T>G
NM_003060.3:c.653-364T>G	NP_003051.1:n.653-364T>G
XM_011543590.1:c.35-364T>G	XP_011541892.1:n.35-364T>G
XR_427718.1:n.1013-364T>G
XR_948290.1:n.994-364T>G
XR_948291.1:n.1007-364T>G
XM_011543590.2:c.35-364T>G	XP_011541892.1:n.35-364T>G
XM_017009778.2:c.125-364T>G	XP_016865267.1:n.125-364T>G
XR_001742215.1:n.994-364T>G
XR_001742216.1:n.1013-364T>G
XR_427718.2:n.1013-364T>G
XR_948290.2:n.994-364T>G
XR_948291.2:n.1007-364T>G
NM_003060.4:c.653-364T>G MANE Select	NP_003051.1:n.653-364T>G
NM_001308122.2:c.725-364T>G	NP_001295051.1:n.725-364T>G