Canonical Allele Identifier: CA1583146112

Gene: SLC22A5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132387028C= , CM000667.2:g.132387028C=	GRCh38
NC_000005.9:g.131722720C= , CM000667.1:g.131722720C=	GRCh37
NC_000005.8:g.131750619C=	NCBI36
NG_008982.1:g.22320C=
NG_008982.2:g.22325C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.669C=	ENSP00000388838.2:p.Phe223=
ENST00000435065.7:c.900C=	ENSP00000402760.2:p.Phe300=
ENST00000448810.6:c.828C=	ENSP00000401860.2:p.Phe276=
ENST00000686757.1:c.847C=	ENSP00000510721.1:p.His283=
ENST00000687740.1:n.3513C=
ENST00000688151.1:n.2138C=
ENST00000689271.1:c.675C=	ENSP00000510797.1:p.Phe225=
ENST00000690900.1:c.799C=	ENSP00000510703.1:p.His267=
ENST00000692212.1:n.772C=
ENST00000692355.1:c.205-1893C=
ENST00000692413.1:c.844-34C=	ENSP00000509374.1:n.844-34C=
ENST00000692825.1:c.896C=	ENSP00000509447.1:n.896C=
ENST00000693308.1:c.876C=	ENSP00000509770.1:p.Phe292=
ENST00000693763.1:n.1988C=
ENST00000245407.8:c.828C= MANE Select	ENSP00000245407.3:p.Phe276=
ENST00000245407.7:c.828C=	ENSP00000245407.3:p.Phe276=
ENST00000415928.5:c.597C=	ENSP00000388838.1:p.Phe199=
ENST00000435065.6:c.900C=	ENSP00000402760.2:p.Phe300=
ENST00000437841.6:c.*143C=	ENSP00000400553.1:n.*143C=
ENST00000448810.5:c.176C=
ENST00000461013.5:n.8250C=
NM_001308122.1:c.900C=	NP_001295051.1:p.Phe300=
NM_003060.3:c.828C=	NP_003051.1:p.Phe276=
XM_011543590.1:c.210C=	XP_011541892.1:p.Phe70=
XR_427718.1:n.1188C=
XR_948290.1:n.1169C=
XR_948291.1:n.1182C=
XM_011543590.2:c.210C=	XP_011541892.1:p.Phe70=
XM_017009778.2:c.300C=	XP_016865267.1:p.Phe100=
XR_001742215.1:n.1169C=
XR_001742216.1:n.1188C=
XR_427718.2:n.1188C=
XR_948290.2:n.1169C=
XR_948291.2:n.1182C=
NM_003060.4:c.828C= MANE Select	NP_003051.1:p.Phe276=
NM_001308122.2:c.900C=	NP_001295051.1:p.Phe300=