Canonical Allele Identifier: CA446332477

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131722726T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132387034T>G , CM000667.2:g.132387034T>G	GRCh38
NC_000005.9:g.131722726T>G , CM000667.1:g.131722726T>G	GRCh37
NC_000005.8:g.131750625T>G	NCBI36
NG_008982.1:g.22326T>G
NG_008982.2:g.22331T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.675T>G	ENSP00000388838.2:p.Pro225=
ENST00000435065.7:c.906T>G	ENSP00000402760.2:p.Pro302=
ENST00000448810.6:c.834T>G	ENSP00000401860.2:p.Pro278=
ENST00000686757.1:c.853T>G	ENSP00000510721.1:p.Ter285Gly
ENST00000687740.1:n.3519T>G
ENST00000688151.1:n.2144T>G
ENST00000689271.1:c.681T>G	ENSP00000510797.1:p.Pro227=
ENST00000690900.1:c.805T>G	ENSP00000510703.1:p.Ter269Gly
ENST00000692212.1:n.778T>G
ENST00000692355.1:c.205-1887T>G
ENST00000692413.1:c.844-28T>G	ENSP00000509374.1:n.844-28T>G
ENST00000692825.1:c.902T>G	ENSP00000509447.1:n.902T>G
ENST00000693308.1:c.882T>G	ENSP00000509770.1:p.Pro294=
ENST00000693763.1:n.1994T>G
ENST00000245407.8:c.834T>G MANE Select	ENSP00000245407.3:p.Pro278=
ENST00000245407.7:c.834T>G	ENSP00000245407.3:p.Pro278=
ENST00000415928.5:c.603T>G	ENSP00000388838.1:p.Pro201=
ENST00000435065.6:c.906T>G	ENSP00000402760.2:p.Pro302=
ENST00000437841.6:c.*149T>G	ENSP00000400553.1:n.*149T>G
ENST00000448810.5:c.182T>G
ENST00000461013.5:n.8256T>G
NM_001308122.1:c.906T>G	NP_001295051.1:p.Pro302=
NM_003060.3:c.834T>G	NP_003051.1:p.Pro278=
XM_011543590.1:c.216T>G	XP_011541892.1:p.Pro72=
XR_427718.1:n.1194T>G
XR_948290.1:n.1175T>G
XR_948291.1:n.1188T>G
XM_011543590.2:c.216T>G	XP_011541892.1:p.Pro72=
XM_017009778.2:c.306T>G	XP_016865267.1:p.Pro102=
XR_001742215.1:n.1175T>G
XR_001742216.1:n.1194T>G
XR_427718.2:n.1194T>G
XR_948290.2:n.1175T>G
XR_948291.2:n.1188T>G
NM_003060.4:c.834T>G MANE Select	NP_003051.1:p.Pro278=
NM_001308122.2:c.906T>G	NP_001295051.1:p.Pro302=