Canonical Allele Identifier: CA1583149591

Gene: SLC22A5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132390455C= , CM000667.2:g.132390455C=	GRCh38
NC_000005.9:g.131726147C= , CM000667.1:g.131726147C=	GRCh37
NC_000005.8:g.131754046C=	NCBI36
NG_008982.1:g.25747C=
NG_008982.2:g.25752C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.894-235C=	ENSP00000388838.2:n.894-235C=
ENST00000435065.7:c.1125-235C=	ENSP00000402760.2:n.1125-235C=
ENST00000448810.6:c.1053-321C=	ENSP00000401860.2:n.1053-321C=
ENST00000685543.1:n.1194-235C=
ENST00000686757.1:c.*217-235C=	ENSP00000510721.1:n.*217-235C=
ENST00000687740.1:n.3738-235C=
ENST00000688151.1:n.2363-235C=
ENST00000689271.1:c.900-235C=	ENSP00000510797.1:n.900-235C=
ENST00000690900.1:c.*217-235C=	ENSP00000510703.1:n.*217-235C=
ENST00000692212.1:n.2430C=
ENST00000692355.1:c.306-235C=
ENST00000692413.1:c.1035-235C=	ENSP00000509374.1:n.1035-235C=
ENST00000692825.1:c.1121-235C=	ENSP00000509447.1:n.1121-235C=
ENST00000693308.1:c.1101-235C=	ENSP00000509770.1:n.1101-235C=
ENST00000693763.1:n.2213-235C=
ENST00000245407.8:c.1053-235C= MANE Select	ENSP00000245407.3:n.1053-235C=
ENST00000245407.7:c.1053-235C=	ENSP00000245407.3:n.1053-235C=
ENST00000435065.6:c.1125-235C=	ENSP00000402760.2:n.1125-235C=
ENST00000447841.5:c.111+1434C=
ENST00000448810.5:c.401-321C=
ENST00000461013.5:n.8475-235C=
ENST00000475308.1:n.1496C=
ENST00000479605.5:n.156-235C=
NM_001308122.1:c.1125-235C=	NP_001295051.1:n.1125-235C=
NM_003060.3:c.1053-235C=	NP_003051.1:n.1053-235C=
XM_011543590.1:c.435-235C=	XP_011541892.1:n.435-235C=
XR_427718.1:n.1413-235C=
XR_948290.1:n.1393+1434C=
XR_948291.1:n.1407-235C=
XM_011543590.2:c.435-235C=	XP_011541892.1:n.435-235C=
XM_017009778.2:c.525-235C=	XP_016865267.1:n.525-235C=
XR_001742215.1:n.1394-321C=
XR_001742216.1:n.1413-321C=
XR_427718.2:n.1413-235C=
XR_948290.2:n.1393+1434C=
XR_948291.2:n.1407-235C=
NM_003060.4:c.1053-235C= MANE Select	NP_003051.1:n.1053-235C=
NM_001308122.2:c.1125-235C=	NP_001295051.1:n.1125-235C=