Canonical Allele Identifier: CA360803792

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131714173G>T (hg19) ; chr5:g.132378481G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132378481G>T , CM000667.2:g.132378481G>T	GRCh38
NC_000005.9:g.131714173G>T , CM000667.1:g.131714173G>T	GRCh37
NC_000005.8:g.131742072G>T	NCBI36
NG_008982.1:g.13773G>T
NG_008982.2:g.13778G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000415928.6:c.497G>T	ENSP00000388838.2:p.Arg166Met
ENST00000435065.7:c.569G>T	ENSP00000402760.2:p.Arg190Met
ENST00000448810.6:c.497G>T	ENSP00000401860.2:p.Arg166Met
ENST00000686757.1:c.497G>T	ENSP00000510721.1:p.Arg166Met
ENST00000687740.1:n.631G>T
ENST00000689271.1:c.497G>T	ENSP00000510797.1:p.Arg166Met
ENST00000690900.1:c.497G>T	ENSP00000510703.1:p.Arg166Met
ENST00000692355.1:c.49G>T
ENST00000692413.1:c.497G>T	ENSP00000509374.1:p.Arg166Met
ENST00000692825.1:c.565G>T	ENSP00000509447.1:n.565G>T
ENST00000693308.1:c.497G>T	ENSP00000509770.1:p.Arg166Met
ENST00000693763.1:n.631G>T
ENST00000245407.8:c.497G>T MANE Select	ENSP00000245407.3:p.Arg166Met
ENST00000245407.7:c.497G>T	ENSP00000245407.3:p.Arg166Met
ENST00000415928.5:c.266G>T	ENSP00000388838.1:p.Arg89Met
ENST00000435065.6:c.569G>T	ENSP00000402760.2:p.Arg190Met
ENST00000437841.6:c.394-6847G>T	ENSP00000400553.1:n.394-6847G>T
ENST00000461013.5:n.2254G>T
NM_001308122.1:c.569G>T	NP_001295051.1:p.Arg190Met
NM_003060.3:c.497G>T	NP_003051.1:p.Arg166Met
XR_427718.1:n.838G>T
XR_948290.1:n.838G>T
XR_948291.1:n.838G>T
XM_011543590.2:c.-135G>T	XP_011541892.1:n.-135G>T
XM_017009778.2:c.-31-5666G>T	XP_016865267.1:n.-31-5666G>T
XR_001742215.1:n.838G>T
XR_001742216.1:n.838G>T
XR_427718.2:n.838G>T
XR_948290.2:n.838G>T
XR_948291.2:n.838G>T
NM_003060.4:c.497G>T MANE Select	NP_003051.1:p.Arg166Met
NM_001308122.2:c.569G>T	NP_001295051.1:p.Arg190Met