Canonical Allele Identifier: CA1583143661

Gene: SLC22A5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132392606G= , CM000667.2:g.132392606G=	GRCh38
NC_000005.9:g.131728298G= , CM000667.1:g.131728298G=	GRCh37
NC_000005.8:g.131756197G=	NCBI36
NG_008982.1:g.27898G=
NG_008982.2:g.27903G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.1282G=	ENSP00000388838.2:p.Val428=
ENST00000435065.7:c.1513G=	ENSP00000402760.2:p.Val505=
ENST00000448810.6:c.*293G=	ENSP00000401860.2:n.*293G=
ENST00000685543.1:n.1582G=
ENST00000686757.1:c.*605G=	ENSP00000510721.1:n.*605G=
ENST00000687740.1:n.4126G=
ENST00000688151.1:n.2751G=
ENST00000689271.1:c.1288G=	ENSP00000510797.1:p.Val430=
ENST00000690900.1:c.*605G=	ENSP00000510703.1:n.*605G=
ENST00000692212.1:n.4581G=
ENST00000692355.1:c.694G=
ENST00000692413.1:c.1423G=	ENSP00000509374.1:p.Val475=
ENST00000692825.1:c.1509G=	ENSP00000509447.1:n.1509G=
ENST00000693308.1:c.1489G=	ENSP00000509770.1:p.Val497=
ENST00000693763.1:n.2601G=
ENST00000245407.8:c.1441G= MANE Select	ENSP00000245407.3:p.Val481=
ENST00000245407.7:c.1441G=	ENSP00000245407.3:p.Val481=
ENST00000435065.6:c.1513G=	ENSP00000402760.2:p.Val505=
ENST00000447841.5:c.285G=
ENST00000448810.5:c.703G=
ENST00000461013.5:n.8863G=
ENST00000475308.1:n.2119G=
ENST00000479605.5:n.544G=
NM_001308122.1:c.1513G=	NP_001295051.1:p.Val505=
NM_003060.3:c.1441G=	NP_003051.1:p.Val481=
XM_011543590.1:c.823G=	XP_011541892.1:p.Val275=
XR_948290.1:n.1567G=
XM_011543590.2:c.823G=	XP_011541892.1:p.Val275=
XM_017009778.2:c.913G=	XP_016865267.1:p.Val305=
XR_001742215.1:n.1696G=
XR_001742216.1:n.1715G=
XR_427718.2:n.1801G=
XR_948290.2:n.1567G=
XR_948291.2:n.1795G=
NM_003060.4:c.1441G= MANE Select	NP_003051.1:p.Val481=
NM_001308122.2:c.1513G=	NP_001295051.1:p.Val505=