Canonical Allele Identifier: CA1583150251

Gene: SLC22A5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132390875T= , CM000667.2:g.132390875T=	GRCh38
NC_000005.9:g.131726567T= , CM000667.1:g.131726567T=	GRCh37
NC_000005.8:g.131754466T=	NCBI36
NG_008982.1:g.26167T=
NG_008982.2:g.26172T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.1079T=	ENSP00000388838.2:p.Val360=
ENST00000435065.7:c.1310T=	ENSP00000402760.2:p.Val437=
ENST00000448810.6:c.*90T=	ENSP00000401860.2:n.*90T=
ENST00000685543.1:n.1379T=
ENST00000686757.1:c.*402T=	ENSP00000510721.1:n.*402T=
ENST00000687740.1:n.3923T=
ENST00000688151.1:n.2548T=
ENST00000689271.1:c.1085T=	ENSP00000510797.1:p.Val362=
ENST00000690900.1:c.*402T=	ENSP00000510703.1:n.*402T=
ENST00000692212.1:n.2850T=
ENST00000692355.1:c.491T=
ENST00000692413.1:c.1220T=	ENSP00000509374.1:p.Val407=
ENST00000692825.1:c.1306T=	ENSP00000509447.1:n.1306T=
ENST00000693308.1:c.1286T=	ENSP00000509770.1:p.Val429=
ENST00000693763.1:n.2398T=
ENST00000245407.8:c.1238T= MANE Select	ENSP00000245407.3:p.Val413=
ENST00000245407.7:c.1238T=	ENSP00000245407.3:p.Val413=
ENST00000435065.6:c.1310T=	ENSP00000402760.2:p.Val437=
ENST00000447841.5:c.112-1558T=
ENST00000448810.5:c.500T=
ENST00000461013.5:n.8660T=
ENST00000475308.1:n.1916T=
ENST00000479605.5:n.341T=
NM_001308122.1:c.1310T=	NP_001295051.1:p.Val437=
NM_003060.3:c.1238T=	NP_003051.1:p.Val413=
XM_011543590.1:c.620T=	XP_011541892.1:p.Val207=
XR_427718.1:n.1598T=
XR_948290.1:n.1394-1558T=
XR_948291.1:n.1592T=
XM_011543590.2:c.620T=	XP_011541892.1:p.Val207=
XM_017009778.2:c.710T=	XP_016865267.1:p.Val237=
XR_001742215.1:n.1493T=
XR_001742216.1:n.1512T=
XR_427718.2:n.1598T=
XR_948290.2:n.1394-1558T=
XR_948291.2:n.1592T=
NM_003060.4:c.1238T= MANE Select	NP_003051.1:p.Val413=
NM_001308122.2:c.1310T=	NP_001295051.1:p.Val437=