Canonical Allele Identifier: CA1583146086

Gene: SLC22A5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132387017A= , CM000667.2:g.132387017A=	GRCh38
NC_000005.9:g.131722709A= , CM000667.1:g.131722709A=	GRCh37
NC_000005.8:g.131750608A=	NCBI36
NG_008982.1:g.22309A=
NG_008982.2:g.22314A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.666-8A=	ENSP00000388838.2:n.666-8A=
ENST00000435065.7:c.897-8A=	ENSP00000402760.2:n.897-8A=
ENST00000448810.6:c.825-8A=	ENSP00000401860.2:n.825-8A=
ENST00000686757.1:c.844-8A=	ENSP00000510721.1:n.844-8A=
ENST00000687740.1:n.3502A=
ENST00000688151.1:n.2135-8A=
ENST00000689271.1:c.672-8A=	ENSP00000510797.1:n.672-8A=
ENST00000690900.1:c.796-8A=	ENSP00000510703.1:n.796-8A=
ENST00000692212.1:n.769-8A=
ENST00000692355.1:c.205-1904A=
ENST00000692413.1:c.844-45A=	ENSP00000509374.1:n.844-45A=
ENST00000692825.1:c.893-8A=	ENSP00000509447.1:n.893-8A=
ENST00000693308.1:c.865A=	ENSP00000509770.1:p.Thr289=
ENST00000693763.1:n.1985-8A=
ENST00000245407.8:c.825-8A= MANE Select	ENSP00000245407.3:n.825-8A=
ENST00000245407.7:c.825-8A=	ENSP00000245407.3:n.825-8A=
ENST00000415928.5:c.594-8A=	ENSP00000388838.1:n.594-8A=
ENST00000435065.6:c.897-8A=	ENSP00000402760.2:n.897-8A=
ENST00000437841.6:c.*140-8A=	ENSP00000400553.1:n.*140-8A=
ENST00000448810.5:c.173-8A=
ENST00000461013.5:n.8247-8A=
NM_001308122.1:c.897-8A=	NP_001295051.1:n.897-8A=
NM_003060.3:c.825-8A=	NP_003051.1:n.825-8A=
XM_011543590.1:c.207-8A=	XP_011541892.1:n.207-8A=
XR_427718.1:n.1185-8A=
XR_948290.1:n.1166-8A=
XR_948291.1:n.1179-8A=
XM_011543590.2:c.207-8A=	XP_011541892.1:n.207-8A=
XM_017009778.2:c.297-8A=	XP_016865267.1:n.297-8A=
XR_001742215.1:n.1166-8A=
XR_001742216.1:n.1185-8A=
XR_427718.2:n.1185-8A=
XR_948290.2:n.1166-8A=
XR_948291.2:n.1179-8A=
NM_003060.4:c.825-8A= MANE Select	NP_003051.1:n.825-8A=
NM_001308122.2:c.897-8A=	NP_001295051.1:n.897-8A=