Canonical Allele Identifier: CA360805160

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131721127C>G (hg19) ; chr5:g.132385435C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132385435C>G , CM000667.2:g.132385435C>G	GRCh38
NC_000005.9:g.131721127C>G , CM000667.1:g.131721127C>G	GRCh37
NC_000005.8:g.131749026C>G	NCBI36
NG_008982.1:g.20727C>G
NG_008982.2:g.20732C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000415928.6:c.665+1121C>G	ENSP00000388838.2:n.665+1121C>G
ENST00000435065.7:c.832C>G	ENSP00000402760.2:p.Arg278Gly
ENST00000448810.6:c.760C>G	ENSP00000401860.2:p.Arg254Gly
ENST00000686757.1:c.779C>G	ENSP00000510721.1:p.Pro260Arg
ENST00000687740.1:n.1920C>G
ENST00000688151.1:n.1952C>G
ENST00000689271.1:c.671+1115C>G	ENSP00000510797.1:n.671+1115C>G
ENST00000690900.1:c.731C>G	ENSP00000510703.1:p.Pro244Arg
ENST00000692212.1:n.586C>G
ENST00000692355.1:c.204+1134C>G
ENST00000692413.1:c.779C>G	ENSP00000509374.1:p.Pro260Arg
ENST00000692825.1:c.828C>G	ENSP00000509447.1:n.828C>G
ENST00000693308.1:c.773C>G	ENSP00000509770.1:p.Pro258Arg
ENST00000693763.1:n.1920C>G
ENST00000245407.8:c.760C>G MANE Select	ENSP00000245407.3:p.Arg254Gly
ENST00000245407.7:c.760C>G	ENSP00000245407.3:p.Arg254Gly
ENST00000415928.5:c.529C>G	ENSP00000388838.1:p.Arg177Gly
ENST00000435065.6:c.832C>G	ENSP00000402760.2:p.Arg278Gly
ENST00000437841.6:c.*75C>G	ENSP00000400553.1:n.*75C>G
ENST00000448810.5:c.108C>G
ENST00000461013.5:n.8182C>G
NM_001308122.1:c.832C>G	NP_001295051.1:p.Arg278Gly
NM_003060.3:c.760C>G	NP_003051.1:p.Arg254Gly
XM_011543590.1:c.142C>G	XP_011541892.1:p.Arg48Gly
XR_427718.1:n.1120C>G
XR_948290.1:n.1101C>G
XR_948291.1:n.1114C>G
XM_011543590.2:c.142C>G	XP_011541892.1:p.Arg48Gly
XM_017009778.2:c.232C>G	XP_016865267.1:p.Arg78Gly
XR_001742215.1:n.1101C>G
XR_001742216.1:n.1120C>G
XR_427718.2:n.1120C>G
XR_948290.2:n.1101C>G
XR_948291.2:n.1114C>G
NM_003060.4:c.760C>G MANE Select	NP_003051.1:p.Arg254Gly
NM_001308122.2:c.832C>G	NP_001295051.1:p.Arg278Gly