Canonical Allele Identifier: CA360805052

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131721079T>G (hg19) ; chr5:g.132385387T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132385387T>G , CM000667.2:g.132385387T>G	GRCh38
NC_000005.9:g.131721079T>G , CM000667.1:g.131721079T>G	GRCh37
NC_000005.8:g.131748978T>G	NCBI36
NG_008982.1:g.20679T>G
NG_008982.2:g.20684T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000415928.6:c.665+1073T>G	ENSP00000388838.2:n.665+1073T>G
ENST00000435065.7:c.784T>G	ENSP00000402760.2:p.Phe262Val
ENST00000448810.6:c.712T>G	ENSP00000401860.2:p.Phe238Val
ENST00000686757.1:c.731T>G	ENSP00000510721.1:p.Ile244Ser
ENST00000687740.1:n.1872T>G
ENST00000688151.1:n.1904T>G
ENST00000689271.1:c.671+1067T>G	ENSP00000510797.1:n.671+1067T>G
ENST00000690900.1:c.683T>G	ENSP00000510703.1:p.Ile228Ser
ENST00000692212.1:n.538T>G
ENST00000692355.1:c.204+1086T>G
ENST00000692413.1:c.731T>G	ENSP00000509374.1:p.Ile244Ser
ENST00000692825.1:c.780T>G	ENSP00000509447.1:n.780T>G
ENST00000693308.1:c.725T>G	ENSP00000509770.1:p.Ile242Ser
ENST00000693763.1:n.1872T>G
ENST00000245407.8:c.712T>G MANE Select	ENSP00000245407.3:p.Phe238Val
ENST00000245407.7:c.712T>G	ENSP00000245407.3:p.Phe238Val
ENST00000415928.5:c.481T>G	ENSP00000388838.1:p.Phe161Val
ENST00000435065.6:c.784T>G	ENSP00000402760.2:p.Phe262Val
ENST00000437841.6:c.*27T>G	ENSP00000400553.1:n.*27T>G
ENST00000448810.5:c.60T>G
ENST00000461013.5:n.8134T>G
NM_001308122.1:c.784T>G	NP_001295051.1:p.Phe262Val
NM_003060.3:c.712T>G	NP_003051.1:p.Phe238Val
XM_011543590.1:c.94T>G	XP_011541892.1:p.Phe32Val
XR_427718.1:n.1072T>G
XR_948290.1:n.1053T>G
XR_948291.1:n.1066T>G
XM_011543590.2:c.94T>G	XP_011541892.1:p.Phe32Val
XM_017009778.2:c.184T>G	XP_016865267.1:p.Phe62Val
XR_001742215.1:n.1053T>G
XR_001742216.1:n.1072T>G
XR_427718.2:n.1072T>G
XR_948290.2:n.1053T>G
XR_948291.2:n.1066T>G
NM_003060.4:c.712T>G MANE Select	NP_003051.1:p.Phe238Val
NM_001308122.2:c.784T>G	NP_001295051.1:p.Phe262Val