Canonical Allele Identifier: CA1583150309

Gene: SLC22A5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132390901C= , CM000667.2:g.132390901C=	GRCh38
NC_000005.9:g.131726593C= , CM000667.1:g.131726593C=	GRCh37
NC_000005.8:g.131754492C=	NCBI36
NG_008982.1:g.26193C=
NG_008982.2:g.26198C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.1105C=	ENSP00000388838.2:p.Pro369=
ENST00000435065.7:c.1336C=	ENSP00000402760.2:p.Pro446=
ENST00000448810.6:c.*116C=	ENSP00000401860.2:n.*116C=
ENST00000685543.1:n.1405C=
ENST00000686757.1:c.*428C=	ENSP00000510721.1:n.*428C=
ENST00000687740.1:n.3949C=
ENST00000688151.1:n.2574C=
ENST00000689271.1:c.1111C=	ENSP00000510797.1:p.Pro371=
ENST00000690900.1:c.*428C=	ENSP00000510703.1:n.*428C=
ENST00000692212.1:n.2876C=
ENST00000692355.1:c.517C=
ENST00000692413.1:c.1246C=	ENSP00000509374.1:p.Pro416=
ENST00000692825.1:c.1332C=	ENSP00000509447.1:n.1332C=
ENST00000693308.1:c.1312C=	ENSP00000509770.1:p.Pro438=
ENST00000693763.1:n.2424C=
ENST00000245407.8:c.1264C= MANE Select	ENSP00000245407.3:p.Pro422=
ENST00000245407.7:c.1264C=	ENSP00000245407.3:p.Pro422=
ENST00000435065.6:c.1336C=	ENSP00000402760.2:p.Pro446=
ENST00000447841.5:c.112-1532C=
ENST00000448810.5:c.526C=
ENST00000461013.5:n.8686C=
ENST00000475308.1:n.1942C=
ENST00000479605.5:n.367C=
NM_001308122.1:c.1336C=	NP_001295051.1:p.Pro446=
NM_003060.3:c.1264C=	NP_003051.1:p.Pro422=
XM_011543590.1:c.646C=	XP_011541892.1:p.Pro216=
XR_427718.1:n.1624C=
XR_948290.1:n.1394-1532C=
XR_948291.1:n.1618C=
XM_011543590.2:c.646C=	XP_011541892.1:p.Pro216=
XM_017009778.2:c.736C=	XP_016865267.1:p.Pro246=
XR_001742215.1:n.1519C=
XR_001742216.1:n.1538C=
XR_427718.2:n.1624C=
XR_948290.2:n.1394-1532C=
XR_948291.2:n.1618C=
NM_003060.4:c.1264C= MANE Select	NP_003051.1:p.Pro422=
NM_001308122.2:c.1336C=	NP_001295051.1:p.Pro446=