Canonical Allele Identifier: CA1583151837

Gene: SLC22A5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132392501G= , CM000667.2:g.132392501G=	GRCh38
NC_000005.9:g.131728193G= , CM000667.1:g.131728193G=	GRCh37
NC_000005.8:g.131756092G=	NCBI36
NG_008982.1:g.27793G=
NG_008982.2:g.27798G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000415928.6:c.1177G=	ENSP00000388838.2:p.Val393=
ENST00000435065.7:c.1408G=	ENSP00000402760.2:p.Val470=
ENST00000448810.6:c.*188G=	ENSP00000401860.2:n.*188G=
ENST00000685543.1:n.1477G=
ENST00000686757.1:c.*500G=	ENSP00000510721.1:n.*500G=
ENST00000687740.1:n.4021G=
ENST00000688151.1:n.2646G=
ENST00000689271.1:c.1183G=	ENSP00000510797.1:p.Val395=
ENST00000690900.1:c.*500G=	ENSP00000510703.1:n.*500G=
ENST00000692212.1:n.4476G=
ENST00000692355.1:c.589G=
ENST00000692413.1:c.1318G=	ENSP00000509374.1:p.Val440=
ENST00000692825.1:c.1404G=	ENSP00000509447.1:n.1404G=
ENST00000693308.1:c.1384G=	ENSP00000509770.1:p.Val462=
ENST00000693763.1:n.2496G=
ENST00000245407.8:c.1336G= MANE Select	ENSP00000245407.3:p.Val446=
ENST00000245407.7:c.1336G=	ENSP00000245407.3:p.Val446=
ENST00000435065.6:c.1408G=	ENSP00000402760.2:p.Val470=
ENST00000447841.5:c.180G=
ENST00000448810.5:c.598G=
ENST00000461013.5:n.8758G=
ENST00000475308.1:n.2014G=
ENST00000479605.5:n.439G=
NM_001308122.1:c.1408G=	NP_001295051.1:p.Val470=
NM_003060.3:c.1336G=	NP_003051.1:p.Val446=
XM_011543590.1:c.718G=	XP_011541892.1:p.Val240=
XR_948290.1:n.1462G=
XM_011543590.2:c.718G=	XP_011541892.1:p.Val240=
XM_017009778.2:c.808G=	XP_016865267.1:p.Val270=
XR_001742215.1:n.1591G=
XR_001742216.1:n.1610G=
XR_427718.2:n.1696G=
XR_948290.2:n.1462G=
XR_948291.2:n.1690G=
NM_003060.4:c.1336G= MANE Select	NP_003051.1:p.Val446=
NM_001308122.2:c.1408G=	NP_001295051.1:p.Val470=