Canonical Allele Identifier: CA1583149948

Gene: SLC22A5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132390733C= , CM000667.2:g.132390733C=	GRCh38
NC_000005.9:g.131726425C= , CM000667.1:g.131726425C=	GRCh37
NC_000005.8:g.131754324C=	NCBI36
NG_008982.1:g.26025C=
NG_008982.2:g.26030C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000415928.6:c.937C=	ENSP00000388838.2:p.Pro313=
ENST00000435065.7:c.1168C=	ENSP00000402760.2:p.Pro390=
ENST00000448810.6:c.1053-43C=	ENSP00000401860.2:n.1053-43C=
ENST00000685543.1:n.1237C=
ENST00000686757.1:c.*260C=	ENSP00000510721.1:n.*260C=
ENST00000687740.1:n.3781C=
ENST00000688151.1:n.2406C=
ENST00000689271.1:c.943C=	ENSP00000510797.1:p.Pro315=
ENST00000690900.1:c.*260C=	ENSP00000510703.1:n.*260C=
ENST00000692212.1:n.2708C=
ENST00000692355.1:c.349C=
ENST00000692413.1:c.1078C=	ENSP00000509374.1:p.Pro360=
ENST00000692825.1:c.1164C=	ENSP00000509447.1:n.1164C=
ENST00000693308.1:c.1144C=	ENSP00000509770.1:p.Pro382=
ENST00000693763.1:n.2256C=
ENST00000245407.8:c.1096C= MANE Select	ENSP00000245407.3:p.Pro366=
ENST00000245407.7:c.1096C=	ENSP00000245407.3:p.Pro366=
ENST00000435065.6:c.1168C=	ENSP00000402760.2:p.Pro390=
ENST00000447841.5:c.112-1700C=
ENST00000448810.5:c.401-43C=
ENST00000461013.5:n.8518C=
ENST00000475308.1:n.1774C=
ENST00000479605.5:n.199C=
NM_001308122.1:c.1168C=	NP_001295051.1:p.Pro390=
NM_003060.3:c.1096C=	NP_003051.1:p.Pro366=
XM_011543590.1:c.478C=	XP_011541892.1:p.Pro160=
XR_427718.1:n.1456C=
XR_948290.1:n.1394-1700C=
XR_948291.1:n.1450C=
XM_011543590.2:c.478C=	XP_011541892.1:p.Pro160=
XM_017009778.2:c.568C=	XP_016865267.1:p.Pro190=
XR_001742215.1:n.1394-43C=
XR_001742216.1:n.1413-43C=
XR_427718.2:n.1456C=
XR_948290.2:n.1394-1700C=
XR_948291.2:n.1450C=
NM_003060.4:c.1096C= MANE Select	NP_003051.1:p.Pro366=
NM_001308122.2:c.1168C=	NP_001295051.1:p.Pro390=