Canonical Allele Identifier: CA360805514

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131722724C>A (hg19) ; chr5:g.132387032C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132387032C>A , CM000667.2:g.132387032C>A	GRCh38
NC_000005.9:g.131722724C>A , CM000667.1:g.131722724C>A	GRCh37
NC_000005.8:g.131750623C>A	NCBI36
NG_008982.1:g.22324C>A
NG_008982.2:g.22329C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.673C>A	ENSP00000388838.2:p.Pro225Thr
ENST00000435065.7:c.904C>A	ENSP00000402760.2:p.Pro302Thr
ENST00000448810.6:c.832C>A	ENSP00000401860.2:p.Pro278Thr
ENST00000686757.1:c.851C>A	ENSP00000510721.1:p.Pro284His
ENST00000687740.1:n.3517C>A
ENST00000688151.1:n.2142C>A
ENST00000689271.1:c.679C>A	ENSP00000510797.1:p.Pro227Thr
ENST00000690900.1:c.803C>A	ENSP00000510703.1:p.Pro268His
ENST00000692212.1:n.776C>A
ENST00000692355.1:c.205-1889C>A
ENST00000692413.1:c.844-30C>A	ENSP00000509374.1:n.844-30C>A
ENST00000692825.1:c.900C>A	ENSP00000509447.1:n.900C>A
ENST00000693308.1:c.880C>A	ENSP00000509770.1:p.Pro294Thr
ENST00000693763.1:n.1992C>A
ENST00000245407.8:c.832C>A MANE Select	ENSP00000245407.3:p.Pro278Thr
ENST00000245407.7:c.832C>A	ENSP00000245407.3:p.Pro278Thr
ENST00000415928.5:c.601C>A	ENSP00000388838.1:p.Pro201Thr
ENST00000435065.6:c.904C>A	ENSP00000402760.2:p.Pro302Thr
ENST00000437841.6:c.*147C>A	ENSP00000400553.1:n.*147C>A
ENST00000448810.5:c.180C>A
ENST00000461013.5:n.8254C>A
NM_001308122.1:c.904C>A	NP_001295051.1:p.Pro302Thr
NM_003060.3:c.832C>A	NP_003051.1:p.Pro278Thr
XM_011543590.1:c.214C>A	XP_011541892.1:p.Pro72Thr
XR_427718.1:n.1192C>A
XR_948290.1:n.1173C>A
XR_948291.1:n.1186C>A
XM_011543590.2:c.214C>A	XP_011541892.1:p.Pro72Thr
XM_017009778.2:c.304C>A	XP_016865267.1:p.Pro102Thr
XR_001742215.1:n.1173C>A
XR_001742216.1:n.1192C>A
XR_427718.2:n.1192C>A
XR_948290.2:n.1173C>A
XR_948291.2:n.1186C>A
NM_003060.4:c.832C>A MANE Select	NP_003051.1:p.Pro278Thr
NM_001308122.2:c.904C>A	NP_001295051.1:p.Pro302Thr