Canonical Allele Identifier: CA3404033

Gene: SLC22A5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132388907T>C , CM000667.2:g.132388907T>C	GRCh38
NC_000005.9:g.131724599T>C , CM000667.1:g.131724599T>C	GRCh37
NC_000005.8:g.131752498T>C	NCBI36
NG_008982.1:g.24199T>C
NG_008982.2:g.24204T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.793-14T>C	ENSP00000388838.2:n.793-14T>C
ENST00000435065.7:c.1024-14T>C	ENSP00000402760.2:n.1024-14T>C
ENST00000448810.6:c.952-14T>C	ENSP00000401860.2:n.952-14T>C
ENST00000685543.1:n.1079T>C
ENST00000686757.1:c.*116-14T>C	ENSP00000510721.1:n.*116-14T>C
ENST00000687740.1:n.3637-14T>C
ENST00000688151.1:n.2262-14T>C
ENST00000689271.1:c.799-14T>C	ENSP00000510797.1:n.799-14T>C
ENST00000690900.1:c.*116-14T>C	ENSP00000510703.1:n.*116-14T>C
ENST00000692212.1:n.896-14T>C
ENST00000692355.1:c.205-14T>C
ENST00000692413.1:c.934-14T>C	ENSP00000509374.1:n.934-14T>C
ENST00000692825.1:c.1020-14T>C	ENSP00000509447.1:n.1020-14T>C
ENST00000693308.1:c.1000-14T>C	ENSP00000509770.1:n.1000-14T>C
ENST00000693763.1:n.2112-14T>C
ENST00000245407.8:c.952-14T>C MANE Select	ENSP00000245407.3:n.952-14T>C
ENST00000245407.7:c.952-14T>C	ENSP00000245407.3:n.952-14T>C
ENST00000435065.6:c.1024-14T>C	ENSP00000402760.2:n.1024-14T>C
ENST00000437841.6:c.*267-14T>C	ENSP00000400553.1:n.*267-14T>C
ENST00000448810.5:c.300-14T>C
ENST00000461013.5:n.8374-14T>C
ENST00000479605.5:n.55-14T>C
NM_001308122.1:c.1024-14T>C	NP_001295051.1:n.1024-14T>C
NM_003060.3:c.952-14T>C	NP_003051.1:n.952-14T>C
XM_011543590.1:c.334-14T>C	XP_011541892.1:n.334-14T>C
XR_427718.1:n.1312-14T>C
XR_948290.1:n.1293-14T>C
XR_948291.1:n.1306-14T>C
XM_011543590.2:c.334-14T>C	XP_011541892.1:n.334-14T>C
XM_017009778.2:c.424-14T>C	XP_016865267.1:n.424-14T>C
XR_001742215.1:n.1293-14T>C
XR_001742216.1:n.1312-14T>C
XR_427718.2:n.1312-14T>C
XR_948290.2:n.1293-14T>C
XR_948291.2:n.1306-14T>C
NM_003060.4:c.952-14T>C MANE Select	NP_003051.1:n.952-14T>C
NM_001308122.2:c.1024-14T>C	NP_001295051.1:n.1024-14T>C