Canonical Allele Identifier: CA360807635

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131726482C>A (hg19) ; chr5:g.132390790C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132390790C>A , CM000667.2:g.132390790C>A	GRCh38
NC_000005.9:g.131726482C>A , CM000667.1:g.131726482C>A	GRCh37
NC_000005.8:g.131754381C>A	NCBI36
NG_008982.1:g.26082C>A
NG_008982.2:g.26087C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.994C>A	ENSP00000388838.2:p.Pro332Thr
ENST00000435065.7:c.1225C>A	ENSP00000402760.2:p.Pro409Thr
ENST00000448810.6:c.*5C>A	ENSP00000401860.2:n.*5C>A
ENST00000685543.1:n.1294C>A
ENST00000686757.1:c.*317C>A	ENSP00000510721.1:n.*317C>A
ENST00000687740.1:n.3838C>A
ENST00000688151.1:n.2463C>A
ENST00000689271.1:c.1000C>A	ENSP00000510797.1:p.Pro334Thr
ENST00000690900.1:c.*317C>A	ENSP00000510703.1:n.*317C>A
ENST00000692212.1:n.2765C>A
ENST00000692355.1:c.406C>A
ENST00000692413.1:c.1135C>A	ENSP00000509374.1:p.Pro379Thr
ENST00000692825.1:c.1221C>A	ENSP00000509447.1:n.1221C>A
ENST00000693308.1:c.1201C>A	ENSP00000509770.1:p.Pro401Thr
ENST00000693763.1:n.2313C>A
ENST00000245407.8:c.1153C>A MANE Select	ENSP00000245407.3:p.Pro385Thr
ENST00000245407.7:c.1153C>A	ENSP00000245407.3:p.Pro385Thr
ENST00000435065.6:c.1225C>A	ENSP00000402760.2:p.Pro409Thr
ENST00000447841.5:c.112-1643C>A
ENST00000448810.5:c.415C>A
ENST00000461013.5:n.8575C>A
ENST00000475308.1:n.1831C>A
ENST00000479605.5:n.256C>A
NM_001308122.1:c.1225C>A	NP_001295051.1:p.Pro409Thr
NM_003060.3:c.1153C>A	NP_003051.1:p.Pro385Thr
XM_011543590.1:c.535C>A	XP_011541892.1:p.Pro179Thr
XR_427718.1:n.1513C>A
XR_948290.1:n.1394-1643C>A
XR_948291.1:n.1507C>A
XM_011543590.2:c.535C>A	XP_011541892.1:p.Pro179Thr
XM_017009778.2:c.625C>A	XP_016865267.1:p.Pro209Thr
XR_001742215.1:n.1408C>A
XR_001742216.1:n.1427C>A
XR_427718.2:n.1513C>A
XR_948290.2:n.1394-1643C>A
XR_948291.2:n.1507C>A
NM_003060.4:c.1153C>A MANE Select	NP_003051.1:p.Pro385Thr
NM_001308122.2:c.1225C>A	NP_001295051.1:p.Pro409Thr