Canonical Allele Identifier: CA360805517

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131722725C>G (hg19) ; chr5:g.132387033C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132387033C>G , CM000667.2:g.132387033C>G	GRCh38
NC_000005.9:g.131722725C>G , CM000667.1:g.131722725C>G	GRCh37
NC_000005.8:g.131750624C>G	NCBI36
NG_008982.1:g.22325C>G
NG_008982.2:g.22330C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.674C>G	ENSP00000388838.2:p.Pro225Arg
ENST00000435065.7:c.905C>G	ENSP00000402760.2:p.Pro302Arg
ENST00000448810.6:c.833C>G	ENSP00000401860.2:p.Pro278Arg
ENST00000686757.1:c.852C>G	ENSP00000510721.1:p.Pro284=
ENST00000687740.1:n.3518C>G
ENST00000688151.1:n.2143C>G
ENST00000689271.1:c.680C>G	ENSP00000510797.1:p.Pro227Arg
ENST00000690900.1:c.804C>G	ENSP00000510703.1:p.Pro268=
ENST00000692212.1:n.777C>G
ENST00000692355.1:c.205-1888C>G
ENST00000692413.1:c.844-29C>G	ENSP00000509374.1:n.844-29C>G
ENST00000692825.1:c.901C>G	ENSP00000509447.1:n.901C>G
ENST00000693308.1:c.881C>G	ENSP00000509770.1:p.Pro294Arg
ENST00000693763.1:n.1993C>G
ENST00000245407.8:c.833C>G MANE Select	ENSP00000245407.3:p.Pro278Arg
ENST00000245407.7:c.833C>G	ENSP00000245407.3:p.Pro278Arg
ENST00000415928.5:c.602C>G	ENSP00000388838.1:p.Pro201Arg
ENST00000435065.6:c.905C>G	ENSP00000402760.2:p.Pro302Arg
ENST00000437841.6:c.*148C>G	ENSP00000400553.1:n.*148C>G
ENST00000448810.5:c.181C>G
ENST00000461013.5:n.8255C>G
NM_001308122.1:c.905C>G	NP_001295051.1:p.Pro302Arg
NM_003060.3:c.833C>G	NP_003051.1:p.Pro278Arg
XM_011543590.1:c.215C>G	XP_011541892.1:p.Pro72Arg
XR_427718.1:n.1193C>G
XR_948290.1:n.1174C>G
XR_948291.1:n.1187C>G
XM_011543590.2:c.215C>G	XP_011541892.1:p.Pro72Arg
XM_017009778.2:c.305C>G	XP_016865267.1:p.Pro102Arg
XR_001742215.1:n.1174C>G
XR_001742216.1:n.1193C>G
XR_427718.2:n.1193C>G
XR_948290.2:n.1174C>G
XR_948291.2:n.1187C>G
NM_003060.4:c.833C>G MANE Select	NP_003051.1:p.Pro278Arg
NM_001308122.2:c.905C>G	NP_001295051.1:p.Pro302Arg