Canonical Allele Identifier: CA1583149933

Gene: SLC22A5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132390727G= , CM000667.2:g.132390727G=	GRCh38
NC_000005.9:g.131726419G= , CM000667.1:g.131726419G=	GRCh37
NC_000005.8:g.131754318G=	NCBI36
NG_008982.1:g.26019G=
NG_008982.2:g.26024G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.931G=	ENSP00000388838.2:p.Asp311=
ENST00000435065.7:c.1162G=	ENSP00000402760.2:p.Asp388=
ENST00000448810.6:c.1053-49G=	ENSP00000401860.2:n.1053-49G=
ENST00000685543.1:n.1231G=
ENST00000686757.1:c.*254G=	ENSP00000510721.1:n.*254G=
ENST00000687740.1:n.3775G=
ENST00000688151.1:n.2400G=
ENST00000689271.1:c.937G=	ENSP00000510797.1:p.Asp313=
ENST00000690900.1:c.*254G=	ENSP00000510703.1:n.*254G=
ENST00000692212.1:n.2702G=
ENST00000692355.1:c.343G=
ENST00000692413.1:c.1072G=	ENSP00000509374.1:p.Asp358=
ENST00000692825.1:c.1158G=	ENSP00000509447.1:n.1158G=
ENST00000693308.1:c.1138G=	ENSP00000509770.1:p.Asp380=
ENST00000693763.1:n.2250G=
ENST00000245407.8:c.1090G= MANE Select	ENSP00000245407.3:p.Asp364=
ENST00000245407.7:c.1090G=	ENSP00000245407.3:p.Asp364=
ENST00000435065.6:c.1162G=	ENSP00000402760.2:p.Asp388=
ENST00000447841.5:c.112-1706G=
ENST00000448810.5:c.401-49G=
ENST00000461013.5:n.8512G=
ENST00000475308.1:n.1768G=
ENST00000479605.5:n.193G=
NM_001308122.1:c.1162G=	NP_001295051.1:p.Asp388=
NM_003060.3:c.1090G=	NP_003051.1:p.Asp364=
XM_011543590.1:c.472G=	XP_011541892.1:p.Asp158=
XR_427718.1:n.1450G=
XR_948290.1:n.1394-1706G=
XR_948291.1:n.1444G=
XM_011543590.2:c.472G=	XP_011541892.1:p.Asp158=
XM_017009778.2:c.562G=	XP_016865267.1:p.Asp188=
XR_001742215.1:n.1394-49G=
XR_001742216.1:n.1413-49G=
XR_427718.2:n.1450G=
XR_948290.2:n.1394-1706G=
XR_948291.2:n.1444G=
NM_003060.4:c.1090G= MANE Select	NP_003051.1:p.Asp364=
NM_001308122.2:c.1162G=	NP_001295051.1:p.Asp388=