Canonical Allele Identifier: CA1583151790

Gene: SLC22A5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132392484C= , CM000667.2:g.132392484C=	GRCh38
NC_000005.9:g.131728176C= , CM000667.1:g.131728176C=	GRCh37
NC_000005.8:g.131756075C=	NCBI36
NG_008982.1:g.27776C=
NG_008982.2:g.27781C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.1160C=	ENSP00000388838.2:p.Thr387=
ENST00000435065.7:c.1391C=	ENSP00000402760.2:p.Thr464=
ENST00000448810.6:c.*171C=	ENSP00000401860.2:n.*171C=
ENST00000685543.1:n.1460C=
ENST00000686757.1:c.*483C=	ENSP00000510721.1:n.*483C=
ENST00000687740.1:n.4004C=
ENST00000688151.1:n.2629C=
ENST00000689271.1:c.1166C=	ENSP00000510797.1:p.Thr389=
ENST00000690900.1:c.*483C=	ENSP00000510703.1:n.*483C=
ENST00000692212.1:n.4459C=
ENST00000692355.1:c.572C=
ENST00000692413.1:c.1301C=	ENSP00000509374.1:p.Thr434=
ENST00000692825.1:c.1387C=	ENSP00000509447.1:n.1387C=
ENST00000693308.1:c.1367C=	ENSP00000509770.1:p.Thr456=
ENST00000693763.1:n.2479C=
ENST00000245407.8:c.1319C= MANE Select	ENSP00000245407.3:p.Thr440=
ENST00000245407.7:c.1319C=	ENSP00000245407.3:p.Thr440=
ENST00000435065.6:c.1391C=	ENSP00000402760.2:p.Thr464=
ENST00000447841.5:c.163C=
ENST00000448810.5:c.581C=
ENST00000461013.5:n.8741C=
ENST00000475308.1:n.1997C=
ENST00000479605.5:n.422C=
NM_001308122.1:c.1391C=	NP_001295051.1:p.Thr464=
NM_003060.3:c.1319C=	NP_003051.1:p.Thr440=
XM_011543590.1:c.701C=	XP_011541892.1:p.Thr234=
XR_948290.1:n.1445C=
XM_011543590.2:c.701C=	XP_011541892.1:p.Thr234=
XM_017009778.2:c.791C=	XP_016865267.1:p.Thr264=
XR_001742215.1:n.1574C=
XR_001742216.1:n.1593C=
XR_427718.2:n.1679C=
XR_948290.2:n.1445C=
XR_948291.2:n.1673C=
NM_003060.4:c.1319C= MANE Select	NP_003051.1:p.Thr440=
NM_001308122.2:c.1391C=	NP_001295051.1:p.Thr464=