Canonical Allele Identifier: CA360805269

Gene: SLC22A5

Linked Data

• dbSNP Id: rs2126784070
• MyVariant Identifiers: chr5:g.131721187T>C (hg19) ; chr5:g.132385495T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132385495T>C , CM000667.2:g.132385495T>C	GRCh38
NC_000005.9:g.131721187T>C , CM000667.1:g.131721187T>C	GRCh37
NC_000005.8:g.131749086T>C	NCBI36
NG_008982.1:g.20787T>C
NG_008982.2:g.20792T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.665+1181T>C	ENSP00000388838.2:n.665+1181T>C
ENST00000435065.7:c.892T>C	ENSP00000402760.2:p.Trp298Arg
ENST00000448810.6:c.820T>C	ENSP00000401860.2:p.Trp274Arg
ENST00000686757.1:c.839T>C	ENSP00000510721.1:p.Leu280Pro
ENST00000687740.1:n.1980T>C
ENST00000688151.1:n.2012T>C
ENST00000689271.1:c.671+1175T>C	ENSP00000510797.1:n.671+1175T>C
ENST00000690900.1:c.791T>C	ENSP00000510703.1:p.Leu264Pro
ENST00000692212.1:n.646T>C
ENST00000692355.1:c.204+1194T>C
ENST00000692413.1:c.839T>C	ENSP00000509374.1:p.Leu280Pro
ENST00000692825.1:c.888T>C	ENSP00000509447.1:n.888T>C
ENST00000693308.1:c.833T>C	ENSP00000509770.1:p.Leu278Pro
ENST00000693763.1:n.1980T>C
ENST00000245407.8:c.820T>C MANE Select	ENSP00000245407.3:p.Trp274Arg
ENST00000245407.7:c.820T>C	ENSP00000245407.3:p.Trp274Arg
ENST00000415928.5:c.589T>C	ENSP00000388838.1:p.Trp197Arg
ENST00000435065.6:c.892T>C	ENSP00000402760.2:p.Trp298Arg
ENST00000437841.6:c.*135T>C	ENSP00000400553.1:n.*135T>C
ENST00000448810.5:c.168T>C
ENST00000461013.5:n.8242T>C
NM_001308122.1:c.892T>C	NP_001295051.1:p.Trp298Arg
NM_003060.3:c.820T>C	NP_003051.1:p.Trp274Arg
XM_011543590.1:c.202T>C	XP_011541892.1:p.Trp68Arg
XR_427718.1:n.1180T>C
XR_948290.1:n.1161T>C
XR_948291.1:n.1174T>C
XM_011543590.2:c.202T>C	XP_011541892.1:p.Trp68Arg
XM_017009778.2:c.292T>C	XP_016865267.1:p.Trp98Arg
XR_001742215.1:n.1161T>C
XR_001742216.1:n.1180T>C
XR_427718.2:n.1180T>C
XR_948290.2:n.1161T>C
XR_948291.2:n.1174T>C
NM_003060.4:c.820T>C MANE Select	NP_003051.1:p.Trp274Arg
NM_001308122.2:c.892T>C	NP_001295051.1:p.Trp298Arg