Canonical Allele Identifier: CA1583146207

Gene: SLC22A5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132387053A= , CM000667.2:g.132387053A=	GRCh38
NC_000005.9:g.131722745A= , CM000667.1:g.131722745A=	GRCh37
NC_000005.8:g.131750644A=	NCBI36
NG_008982.1:g.22345A=
NG_008982.2:g.22350A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.694A=	ENSP00000388838.2:p.Ile232=
ENST00000435065.7:c.925A=	ENSP00000402760.2:p.Ile309=
ENST00000448810.6:c.853A=	ENSP00000401860.2:p.Ile285=
ENST00000686757.1:c.*17A=	ENSP00000510721.1:n.*17A=
ENST00000687740.1:n.3538A=
ENST00000688151.1:n.2163A=
ENST00000689271.1:c.700A=	ENSP00000510797.1:p.Ile234=
ENST00000690900.1:c.*17A=	ENSP00000510703.1:n.*17A=
ENST00000692212.1:n.797A=
ENST00000692355.1:c.205-1868A=
ENST00000692413.1:c.844-9A=	ENSP00000509374.1:n.844-9A=
ENST00000692825.1:c.921A=	ENSP00000509447.1:n.921A=
ENST00000693308.1:c.901A=	ENSP00000509770.1:p.Ile301=
ENST00000693763.1:n.2013A=
ENST00000245407.8:c.853A= MANE Select	ENSP00000245407.3:p.Ile285=
ENST00000245407.7:c.853A=	ENSP00000245407.3:p.Ile285=
ENST00000415928.5:c.622A=	ENSP00000388838.1:p.Ile208=
ENST00000435065.6:c.925A=	ENSP00000402760.2:p.Ile309=
ENST00000437841.6:c.*168A=	ENSP00000400553.1:n.*168A=
ENST00000448810.5:c.201A=
ENST00000461013.5:n.8275A=
NM_001308122.1:c.925A=	NP_001295051.1:p.Ile309=
NM_003060.3:c.853A=	NP_003051.1:p.Ile285=
XM_011543590.1:c.235A=	XP_011541892.1:p.Ile79=
XR_427718.1:n.1213A=
XR_948290.1:n.1194A=
XR_948291.1:n.1207A=
XM_011543590.2:c.235A=	XP_011541892.1:p.Ile79=
XM_017009778.2:c.325A=	XP_016865267.1:p.Ile109=
XR_001742215.1:n.1194A=
XR_001742216.1:n.1213A=
XR_427718.2:n.1213A=
XR_948290.2:n.1194A=
XR_948291.2:n.1207A=
NM_003060.4:c.853A= MANE Select	NP_003051.1:p.Ile285=
NM_001308122.2:c.925A=	NP_001295051.1:p.Ile309=