Canonical Allele Identifier: CA360809921

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131729460A>C (hg19) ; chr5:g.132393768A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132393768A>C , CM000667.2:g.132393768A>C	GRCh38
NC_000005.9:g.131729460A>C , CM000667.1:g.131729460A>C	GRCh37
NC_000005.8:g.131757359A>C	NCBI36
NG_008982.1:g.29060A>C
NG_008982.2:g.29065A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.1292-417A>C	ENSP00000388838.2:n.1292-417A>C
ENST00000435065.7:c.1615A>C	ENSP00000402760.2:p.Thr539Pro
ENST00000448810.6:c.*395A>C	ENSP00000401860.2:n.*395A>C
ENST00000685543.1:n.1684A>C
ENST00000686757.1:c.*707A>C	ENSP00000510721.1:n.*707A>C
ENST00000686868.1:n.535A>C
ENST00000687740.1:n.4228A>C
ENST00000688151.1:n.2853A>C
ENST00000689271.1:c.1390A>C	ENSP00000510797.1:p.Thr464Pro
ENST00000690900.1:c.*707A>C	ENSP00000510703.1:n.*707A>C
ENST00000692212.1:n.4683A>C
ENST00000692355.1:c.796A>C
ENST00000692413.1:c.1525A>C	ENSP00000509374.1:p.Thr509Pro
ENST00000692825.1:c.1611A>C	ENSP00000509447.1:n.1611A>C
ENST00000693308.1:c.1591A>C	ENSP00000509770.1:p.Thr531Pro
ENST00000693763.1:n.2703A>C
ENST00000245407.8:c.1543A>C MANE Select	ENSP00000245407.3:p.Thr515Pro
ENST00000245407.7:c.1543A>C	ENSP00000245407.3:p.Thr515Pro
ENST00000435065.6:c.1615A>C	ENSP00000402760.2:p.Thr539Pro
ENST00000447841.5:c.387A>C
ENST00000448810.5:c.805A>C
ENST00000461013.5:n.8965A>C
ENST00000475308.1:n.2221A>C
NM_001308122.1:c.1615A>C	NP_001295051.1:p.Thr539Pro
NM_003060.3:c.1543A>C	NP_003051.1:p.Thr515Pro
XM_011543590.1:c.925A>C	XP_011541892.1:p.Thr309Pro
XR_948290.1:n.1669A>C
XM_011543590.2:c.925A>C	XP_011541892.1:p.Thr309Pro
XM_017009778.2:c.1015A>C	XP_016865267.1:p.Thr339Pro
XR_001742215.1:n.1798A>C
XR_001742216.1:n.1817A>C
XR_427718.2:n.1903A>C
XR_948290.2:n.1669A>C
XR_948291.2:n.1897A>C
NM_003060.4:c.1543A>C MANE Select	NP_003051.1:p.Thr515Pro
NM_001308122.2:c.1615A>C	NP_001295051.1:p.Thr539Pro