Canonical Allele Identifier: CA446340197

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131726589A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132390897A>C , CM000667.2:g.132390897A>C	GRCh38
NC_000005.9:g.131726589A>C , CM000667.1:g.131726589A>C	GRCh37
NC_000005.8:g.131754488A>C	NCBI36
NG_008982.1:g.26189A>C
NG_008982.2:g.26194A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.1101A>C	ENSP00000388838.2:p.Val367=
ENST00000435065.7:c.1332A>C	ENSP00000402760.2:p.Val444=
ENST00000448810.6:c.*112A>C	ENSP00000401860.2:n.*112A>C
ENST00000685543.1:n.1401A>C
ENST00000686757.1:c.*424A>C	ENSP00000510721.1:n.*424A>C
ENST00000687740.1:n.3945A>C
ENST00000688151.1:n.2570A>C
ENST00000689271.1:c.1107A>C	ENSP00000510797.1:p.Val369=
ENST00000690900.1:c.*424A>C	ENSP00000510703.1:n.*424A>C
ENST00000692212.1:n.2872A>C
ENST00000692355.1:c.513A>C
ENST00000692413.1:c.1242A>C	ENSP00000509374.1:p.Val414=
ENST00000692825.1:c.1328A>C	ENSP00000509447.1:n.1328A>C
ENST00000693308.1:c.1308A>C	ENSP00000509770.1:p.Val436=
ENST00000693763.1:n.2420A>C
ENST00000245407.8:c.1260A>C MANE Select	ENSP00000245407.3:p.Val420=
ENST00000245407.7:c.1260A>C	ENSP00000245407.3:p.Val420=
ENST00000435065.6:c.1332A>C	ENSP00000402760.2:p.Val444=
ENST00000447841.5:c.112-1536A>C
ENST00000448810.5:c.522A>C
ENST00000461013.5:n.8682A>C
ENST00000475308.1:n.1938A>C
ENST00000479605.5:n.363A>C
NM_001308122.1:c.1332A>C	NP_001295051.1:p.Val444=
NM_003060.3:c.1260A>C	NP_003051.1:p.Val420=
XM_011543590.1:c.642A>C	XP_011541892.1:p.Val214=
XR_427718.1:n.1620A>C
XR_948290.1:n.1394-1536A>C
XR_948291.1:n.1614A>C
XM_011543590.2:c.642A>C	XP_011541892.1:p.Val214=
XM_017009778.2:c.732A>C	XP_016865267.1:p.Val244=
XR_001742215.1:n.1515A>C
XR_001742216.1:n.1534A>C
XR_427718.2:n.1620A>C
XR_948290.2:n.1394-1536A>C
XR_948291.2:n.1614A>C
NM_003060.4:c.1260A>C MANE Select	NP_003051.1:p.Val420=
NM_001308122.2:c.1332A>C	NP_001295051.1:p.Val444=