Canonical Allele Identifier: CA1583148218

Gene: SLC22A5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132388933A= , CM000667.2:g.132388933A=	GRCh38
NC_000005.9:g.131724625A= , CM000667.1:g.131724625A=	GRCh37
NC_000005.8:g.131752524A=	NCBI36
NG_008982.1:g.24225A=
NG_008982.2:g.24230A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.805A=	ENSP00000388838.2:p.Ser269=
ENST00000435065.7:c.1036A=	ENSP00000402760.2:p.Ser346=
ENST00000448810.6:c.964A=	ENSP00000401860.2:p.Ser322=
ENST00000685543.1:n.1105A=
ENST00000686757.1:c.*128A=	ENSP00000510721.1:n.*128A=
ENST00000687740.1:n.3649A=
ENST00000688151.1:n.2274A=
ENST00000689271.1:c.811A=	ENSP00000510797.1:p.Ser271=
ENST00000690900.1:c.*128A=	ENSP00000510703.1:n.*128A=
ENST00000692212.1:n.908A=
ENST00000692355.1:c.217A=
ENST00000692413.1:c.946A=	ENSP00000509374.1:p.Ser316=
ENST00000692825.1:c.1032A=	ENSP00000509447.1:n.1032A=
ENST00000693308.1:c.1012A=	ENSP00000509770.1:p.Ser338=
ENST00000693763.1:n.2124A=
ENST00000245407.8:c.964A= MANE Select	ENSP00000245407.3:p.Ser322=
ENST00000245407.7:c.964A=	ENSP00000245407.3:p.Ser322=
ENST00000435065.6:c.1036A=	ENSP00000402760.2:p.Ser346=
ENST00000437841.6:c.*279A=	ENSP00000400553.1:n.*279A=
ENST00000447841.5:c.23A=
ENST00000448810.5:c.312A=
ENST00000461013.5:n.8386A=
ENST00000479605.5:n.67A=
NM_001308122.1:c.1036A=	NP_001295051.1:p.Ser346=
NM_003060.3:c.964A=	NP_003051.1:p.Ser322=
XM_011543590.1:c.346A=	XP_011541892.1:p.Ser116=
XR_427718.1:n.1324A=
XR_948290.1:n.1305A=
XR_948291.1:n.1318A=
XM_011543590.2:c.346A=	XP_011541892.1:p.Ser116=
XM_017009778.2:c.436A=	XP_016865267.1:p.Ser146=
XR_001742215.1:n.1305A=
XR_001742216.1:n.1324A=
XR_427718.2:n.1324A=
XR_948290.2:n.1305A=
XR_948291.2:n.1318A=
NM_003060.4:c.964A= MANE Select	NP_003051.1:p.Ser322=
NM_001308122.2:c.1036A=	NP_001295051.1:p.Ser346=