Canonical Allele Identifier: CA1583146162

Gene: SLC22A5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132387045G= , CM000667.2:g.132387045G=	GRCh38
NC_000005.9:g.131722737G= , CM000667.1:g.131722737G=	GRCh37
NC_000005.8:g.131750636G=	NCBI36
NG_008982.1:g.22337G=
NG_008982.2:g.22342G=

Transcript Alleles

HGVS	Amino-acid Change
NM_003060.4:c.845G= MANE Select	NP_003051.1:p.Arg282=
ENST00000245407.8:c.845G= MANE Select	ENSP00000245407.3:p.Arg282=
NM_001308122.1:c.917G=	NP_001295051.1:p.Arg306=
NM_001308122.2:c.917G=	NP_001295051.1:p.Arg306=
NM_003060.3:c.845G=	NP_003051.1:p.Arg282=
ENST00000245407.7:c.845G=	ENSP00000245407.3:p.Arg282=
ENST00000415928.5:c.614G=	ENSP00000388838.1:p.Arg205=
ENST00000415928.6:c.686G=	ENSP00000388838.2:p.Arg229=
ENST00000435065.6:c.917G=	ENSP00000402760.2:p.Arg306=
ENST00000435065.7:c.917G=	ENSP00000402760.2:p.Arg306=
ENST00000437841.6:c.*160G=	ENSP00000400553.1:n.*160G=
ENST00000448810.5:c.193G=
ENST00000448810.6:c.845G=	ENSP00000401860.2:p.Arg282=
ENST00000461013.5:n.8267G=
ENST00000686757.1:c.*9G=	ENSP00000510721.1:n.*9G=
ENST00000687740.1:n.3530G=
ENST00000688151.1:n.2155G=
ENST00000689271.1:c.692G=	ENSP00000510797.1:p.Arg231=
ENST00000690900.1:c.*9G=	ENSP00000510703.1:n.*9G=
ENST00000692212.1:n.789G=
ENST00000692355.1:c.205-1876G=
ENST00000692413.1:c.844-17G=	ENSP00000509374.1:n.844-17G=
ENST00000692825.1:c.913G=	ENSP00000509447.1:n.913G=
ENST00000693308.1:c.893G=	ENSP00000509770.1:p.Arg298=
ENST00000693763.1:n.2005G=
XM_011543590.1:c.227G=	XP_011541892.1:p.Arg76=
XM_011543590.2:c.227G=	XP_011541892.1:p.Arg76=
XM_017009778.2:c.317G=	XP_016865267.1:p.Arg106=
XR_001742215.1:n.1186G=
XR_001742216.1:n.1205G=
XR_427718.1:n.1205G=
XR_427718.2:n.1205G=
XR_948290.1:n.1186G=
XR_948290.2:n.1186G=
XR_948291.1:n.1199G=
XR_948291.2:n.1199G=