Canonical Allele Identifier: CA3123367196

Gene: SLC22A5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132390839A= , CM000667.2:g.132390839A=	GRCh38
NC_000005.9:g.131726531A= , CM000667.1:g.131726531A=	GRCh37
NC_000005.8:g.131754430A=	NCBI36
NG_008982.1:g.26131A=
NG_008982.2:g.26136A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.1043A=	ENSP00000388838.2:p.Tyr348=
ENST00000435065.7:c.1274A=	ENSP00000402760.2:p.Tyr425=
ENST00000448810.6:c.*54A=	ENSP00000401860.2:n.*54A=
ENST00000685543.1:n.1343A=
ENST00000686757.1:c.*366A=	ENSP00000510721.1:n.*366A=
ENST00000687740.1:n.3887A=
ENST00000688151.1:n.2512A=
ENST00000689271.1:c.1049A=	ENSP00000510797.1:p.Tyr350=
ENST00000690900.1:c.*366A=	ENSP00000510703.1:n.*366A=
ENST00000692212.1:n.2814A=
ENST00000692355.1:c.455A=
ENST00000692413.1:c.1184A=	ENSP00000509374.1:p.Tyr395=
ENST00000692825.1:c.1270A=	ENSP00000509447.1:n.1270A=
ENST00000693308.1:c.1250A=	ENSP00000509770.1:p.Tyr417=
ENST00000693763.1:n.2362A=
ENST00000245407.8:c.1202A= MANE Select	ENSP00000245407.3:p.Tyr401=
ENST00000245407.7:c.1202A=	ENSP00000245407.3:p.Tyr401=
ENST00000435065.6:c.1274A=	ENSP00000402760.2:p.Tyr425=
ENST00000447841.5:c.112-1594A=
ENST00000448810.5:c.464A=
ENST00000461013.5:n.8624A=
ENST00000475308.1:n.1880A=
ENST00000479605.5:n.305A=
NM_001308122.1:c.1274A=	NP_001295051.1:p.Tyr425=
NM_003060.3:c.1202A=	NP_003051.1:p.Tyr401=
XM_011543590.1:c.584A=	XP_011541892.1:p.Tyr195=
XR_427718.1:n.1562A=
XR_948290.1:n.1394-1594A=
XR_948291.1:n.1556A=
XM_011543590.2:c.584A=	XP_011541892.1:p.Tyr195=
XM_017009778.2:c.674A=	XP_016865267.1:p.Tyr225=
XR_001742215.1:n.1457A=
XR_001742216.1:n.1476A=
XR_427718.2:n.1562A=
XR_948290.2:n.1394-1594A=
XR_948291.2:n.1556A=
NM_003060.4:c.1202A= MANE Select	NP_003051.1:p.Tyr401=
NM_001308122.2:c.1274A=	NP_001295051.1:p.Tyr425=