Canonical Allele Identifier: CA1583151864

Gene: SLC22A5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132392510T= , CM000667.2:g.132392510T=	GRCh38
NC_000005.9:g.131728202T= , CM000667.1:g.131728202T=	GRCh37
NC_000005.8:g.131756101T=	NCBI36
NG_008982.1:g.27802T=
NG_008982.2:g.27807T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.1186T=	ENSP00000388838.2:p.Tyr396=
ENST00000435065.7:c.1417T=	ENSP00000402760.2:p.Tyr473=
ENST00000448810.6:c.*197T=	ENSP00000401860.2:n.*197T=
ENST00000685543.1:n.1486T=
ENST00000686757.1:c.*509T=	ENSP00000510721.1:n.*509T=
ENST00000687740.1:n.4030T=
ENST00000688151.1:n.2655T=
ENST00000689271.1:c.1192T=	ENSP00000510797.1:p.Tyr398=
ENST00000690900.1:c.*509T=	ENSP00000510703.1:n.*509T=
ENST00000692212.1:n.4485T=
ENST00000692355.1:c.598T=
ENST00000692413.1:c.1327T=	ENSP00000509374.1:p.Tyr443=
ENST00000692825.1:c.1413T=	ENSP00000509447.1:n.1413T=
ENST00000693308.1:c.1393T=	ENSP00000509770.1:p.Tyr465=
ENST00000693763.1:n.2505T=
ENST00000245407.8:c.1345T= MANE Select	ENSP00000245407.3:p.Tyr449=
ENST00000245407.7:c.1345T=	ENSP00000245407.3:p.Tyr449=
ENST00000435065.6:c.1417T=	ENSP00000402760.2:p.Tyr473=
ENST00000447841.5:c.189T=
ENST00000448810.5:c.607T=
ENST00000461013.5:n.8767T=
ENST00000475308.1:n.2023T=
ENST00000479605.5:n.448T=
NM_001308122.1:c.1417T=	NP_001295051.1:p.Tyr473=
NM_003060.3:c.1345T=	NP_003051.1:p.Tyr449=
XM_011543590.1:c.727T=	XP_011541892.1:p.Tyr243=
XR_948290.1:n.1471T=
XM_011543590.2:c.727T=	XP_011541892.1:p.Tyr243=
XM_017009778.2:c.817T=	XP_016865267.1:p.Tyr273=
XR_001742215.1:n.1600T=
XR_001742216.1:n.1619T=
XR_427718.2:n.1705T=
XR_948290.2:n.1471T=
XR_948291.2:n.1699T=
NM_003060.4:c.1345T= MANE Select	NP_003051.1:p.Tyr449=
NM_001308122.2:c.1417T=	NP_001295051.1:p.Tyr473=