Canonical Allele Identifier: CA1583146230

Gene: SLC22A5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132387059C= , CM000667.2:g.132387059C=	GRCh38
NC_000005.9:g.131722751C= , CM000667.1:g.131722751C=	GRCh37
NC_000005.8:g.131750650C=	NCBI36
NG_008982.1:g.22351C=
NG_008982.2:g.22356C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.700C=	ENSP00000388838.2:p.Gln234=
ENST00000435065.7:c.931C=	ENSP00000402760.2:p.Gln311=
ENST00000448810.6:c.859C=	ENSP00000401860.2:p.Gln287=
ENST00000686757.1:c.*23C=	ENSP00000510721.1:n.*23C=
ENST00000687740.1:n.3544C=
ENST00000688151.1:n.2169C=
ENST00000689271.1:c.706C=	ENSP00000510797.1:p.Gln236=
ENST00000690900.1:c.*23C=	ENSP00000510703.1:n.*23C=
ENST00000692212.1:n.803C=
ENST00000692355.1:c.205-1862C=
ENST00000692413.1:c.844-3C=	ENSP00000509374.1:n.844-3C=
ENST00000692825.1:c.927C=	ENSP00000509447.1:n.927C=
ENST00000693308.1:c.907C=	ENSP00000509770.1:p.Gln303=
ENST00000693763.1:n.2019C=
ENST00000245407.8:c.859C= MANE Select	ENSP00000245407.3:p.Gln287=
ENST00000245407.7:c.859C=	ENSP00000245407.3:p.Gln287=
ENST00000415928.5:c.628C=	ENSP00000388838.1:p.Gln210=
ENST00000435065.6:c.931C=	ENSP00000402760.2:p.Gln311=
ENST00000437841.6:c.*174C=	ENSP00000400553.1:n.*174C=
ENST00000448810.5:c.207C=
ENST00000461013.5:n.8281C=
NM_001308122.1:c.931C=	NP_001295051.1:p.Gln311=
NM_003060.3:c.859C=	NP_003051.1:p.Gln287=
XM_011543590.1:c.241C=	XP_011541892.1:p.Gln81=
XR_427718.1:n.1219C=
XR_948290.1:n.1200C=
XR_948291.1:n.1213C=
XM_011543590.2:c.241C=	XP_011541892.1:p.Gln81=
XM_017009778.2:c.331C=	XP_016865267.1:p.Gln111=
XR_001742215.1:n.1200C=
XR_001742216.1:n.1219C=
XR_427718.2:n.1219C=
XR_948290.2:n.1200C=
XR_948291.2:n.1213C=
NM_003060.4:c.859C= MANE Select	NP_003051.1:p.Gln287=
NM_001308122.2:c.931C=	NP_001295051.1:p.Gln311=