Canonical Allele Identifier: CA1583144780

Gene: SLC22A5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132385476G= , CM000667.2:g.132385476G=	GRCh38
NC_000005.9:g.131721168G= , CM000667.1:g.131721168G=	GRCh37
NC_000005.8:g.131749067G=	NCBI36
NG_008982.1:g.20768G=
NG_008982.2:g.20773G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.665+1162G=	ENSP00000388838.2:n.665+1162G=
ENST00000435065.7:c.873G=	ENSP00000402760.2:p.Gly291=
ENST00000448810.6:c.801G=	ENSP00000401860.2:p.Gly267=
ENST00000686757.1:c.820G=	ENSP00000510721.1:p.Gly274=
ENST00000687740.1:n.1961G=
ENST00000688151.1:n.1993G=
ENST00000689271.1:c.671+1156G=	ENSP00000510797.1:n.671+1156G=
ENST00000690900.1:c.772G=	ENSP00000510703.1:p.Gly258=
ENST00000692212.1:n.627G=
ENST00000692355.1:c.204+1175G=
ENST00000692413.1:c.820G=	ENSP00000509374.1:p.Gly274=
ENST00000692825.1:c.869G=	ENSP00000509447.1:n.869G=
ENST00000693308.1:c.814G=	ENSP00000509770.1:p.Gly272=
ENST00000693763.1:n.1961G=
ENST00000245407.8:c.801G= MANE Select	ENSP00000245407.3:p.Gly267=
ENST00000245407.7:c.801G=	ENSP00000245407.3:p.Gly267=
ENST00000415928.5:c.570G=	ENSP00000388838.1:p.Gly190=
ENST00000435065.6:c.873G=	ENSP00000402760.2:p.Gly291=
ENST00000437841.6:c.*116G=	ENSP00000400553.1:n.*116G=
ENST00000448810.5:c.149G=
ENST00000461013.5:n.8223G=
NM_001308122.1:c.873G=	NP_001295051.1:p.Gly291=
NM_003060.3:c.801G=	NP_003051.1:p.Gly267=
XM_011543590.1:c.183G=	XP_011541892.1:p.Gly61=
XR_427718.1:n.1161G=
XR_948290.1:n.1142G=
XR_948291.1:n.1155G=
XM_011543590.2:c.183G=	XP_011541892.1:p.Gly61=
XM_017009778.2:c.273G=	XP_016865267.1:p.Gly91=
XR_001742215.1:n.1142G=
XR_001742216.1:n.1161G=
XR_427718.2:n.1161G=
XR_948290.2:n.1142G=
XR_948291.2:n.1155G=
NM_003060.4:c.801G= MANE Select	NP_003051.1:p.Gly267=
NM_001308122.2:c.873G=	NP_001295051.1:p.Gly291=