Canonical Allele Identifier: CA1583149659

Gene: SLC22A5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132390528T= , CM000667.2:g.132390528T=	GRCh38
NC_000005.9:g.131726220T= , CM000667.1:g.131726220T=	GRCh37
NC_000005.8:g.131754119T=	NCBI36
NG_008982.1:g.25820T=
NG_008982.2:g.25825T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.894-162T=	ENSP00000388838.2:n.894-162T=
ENST00000435065.7:c.1125-162T=	ENSP00000402760.2:n.1125-162T=
ENST00000448810.6:c.1053-248T=	ENSP00000401860.2:n.1053-248T=
ENST00000685543.1:n.1194-162T=
ENST00000686757.1:c.*217-162T=	ENSP00000510721.1:n.*217-162T=
ENST00000687740.1:n.3738-162T=
ENST00000688151.1:n.2363-162T=
ENST00000689271.1:c.900-162T=	ENSP00000510797.1:n.900-162T=
ENST00000690900.1:c.*217-162T=	ENSP00000510703.1:n.*217-162T=
ENST00000692212.1:n.2503T=
ENST00000692355.1:c.306-162T=
ENST00000692413.1:c.1035-162T=	ENSP00000509374.1:n.1035-162T=
ENST00000692825.1:c.1121-162T=	ENSP00000509447.1:n.1121-162T=
ENST00000693308.1:c.1101-162T=	ENSP00000509770.1:n.1101-162T=
ENST00000693763.1:n.2213-162T=
ENST00000245407.8:c.1053-162T= MANE Select	ENSP00000245407.3:n.1053-162T=
ENST00000245407.7:c.1053-162T=	ENSP00000245407.3:n.1053-162T=
ENST00000435065.6:c.1125-162T=	ENSP00000402760.2:n.1125-162T=
ENST00000447841.5:c.111+1507T=
ENST00000448810.5:c.401-248T=
ENST00000461013.5:n.8475-162T=
ENST00000475308.1:n.1569T=
ENST00000479605.5:n.156-162T=
NM_001308122.1:c.1125-162T=	NP_001295051.1:n.1125-162T=
NM_003060.3:c.1053-162T=	NP_003051.1:n.1053-162T=
XM_011543590.1:c.435-162T=	XP_011541892.1:n.435-162T=
XR_427718.1:n.1413-162T=
XR_948290.1:n.1393+1507T=
XR_948291.1:n.1407-162T=
XM_011543590.2:c.435-162T=	XP_011541892.1:n.435-162T=
XM_017009778.2:c.525-162T=	XP_016865267.1:n.525-162T=
XR_001742215.1:n.1394-248T=
XR_001742216.1:n.1413-248T=
XR_427718.2:n.1413-162T=
XR_948290.2:n.1393+1507T=
XR_948291.2:n.1407-162T=
NM_003060.4:c.1053-162T= MANE Select	NP_003051.1:n.1053-162T=
NM_001308122.2:c.1125-162T=	NP_001295051.1:n.1125-162T=