Canonical Allele Identifier: CA1583149898

Gene: SLC22A5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132390717G= , CM000667.2:g.132390717G=	GRCh38
NC_000005.9:g.131726409G= , CM000667.1:g.131726409G=	GRCh37
NC_000005.8:g.131754308G=	NCBI36
NG_008982.1:g.26009G=
NG_008982.2:g.26014G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.921G=	ENSP00000388838.2:p.Gly307=
ENST00000435065.7:c.1152G=	ENSP00000402760.2:p.Gly384=
ENST00000448810.6:c.1053-59G=	ENSP00000401860.2:n.1053-59G=
ENST00000685543.1:n.1221G=
ENST00000686757.1:c.*244G=	ENSP00000510721.1:n.*244G=
ENST00000687740.1:n.3765G=
ENST00000688151.1:n.2390G=
ENST00000689271.1:c.927G=	ENSP00000510797.1:p.Gly309=
ENST00000690900.1:c.*244G=	ENSP00000510703.1:n.*244G=
ENST00000692212.1:n.2692G=
ENST00000692355.1:c.333G=
ENST00000692413.1:c.1062G=	ENSP00000509374.1:p.Gly354=
ENST00000692825.1:c.1148G=	ENSP00000509447.1:n.1148G=
ENST00000693308.1:c.1128G=	ENSP00000509770.1:p.Gly376=
ENST00000693763.1:n.2240G=
ENST00000245407.8:c.1080G= MANE Select	ENSP00000245407.3:p.Gly360=
ENST00000245407.7:c.1080G=	ENSP00000245407.3:p.Gly360=
ENST00000435065.6:c.1152G=	ENSP00000402760.2:p.Gly384=
ENST00000447841.5:c.111+1696G=
ENST00000448810.5:c.401-59G=
ENST00000461013.5:n.8502G=
ENST00000475308.1:n.1758G=
ENST00000479605.5:n.183G=
NM_001308122.1:c.1152G=	NP_001295051.1:p.Gly384=
NM_003060.3:c.1080G=	NP_003051.1:p.Gly360=
XM_011543590.1:c.462G=	XP_011541892.1:p.Gly154=
XR_427718.1:n.1440G=
XR_948290.1:n.1393+1696G=
XR_948291.1:n.1434G=
XM_011543590.2:c.462G=	XP_011541892.1:p.Gly154=
XM_017009778.2:c.552G=	XP_016865267.1:p.Gly184=
XR_001742215.1:n.1394-59G=
XR_001742216.1:n.1413-59G=
XR_427718.2:n.1440G=
XR_948290.2:n.1393+1696G=
XR_948291.2:n.1434G=
NM_003060.4:c.1080G= MANE Select	NP_003051.1:p.Gly360=
NM_001308122.2:c.1152G=	NP_001295051.1:p.Gly384=