Canonical Allele Identifier: CA360807637

Gene: SLC22A5

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.994C>G	ENSP00000388838.2:p.Pro332Ala
ENST00000435065.7:c.1225C>G	ENSP00000402760.2:p.Pro409Ala
ENST00000448810.6:c.*5C>G	ENSP00000401860.2:n.*5C>G
ENST00000685543.1:n.1294C>G
ENST00000686757.1:c.*317C>G	ENSP00000510721.1:n.*317C>G
ENST00000687740.1:n.3838C>G
ENST00000688151.1:n.2463C>G
ENST00000689271.1:c.1000C>G	ENSP00000510797.1:p.Pro334Ala
ENST00000690900.1:c.*317C>G	ENSP00000510703.1:n.*317C>G
ENST00000692212.1:n.2765C>G
ENST00000692355.1:c.406C>G
ENST00000692413.1:c.1135C>G	ENSP00000509374.1:p.Pro379Ala
ENST00000692825.1:c.1221C>G	ENSP00000509447.1:n.1221C>G
ENST00000693308.1:c.1201C>G	ENSP00000509770.1:p.Pro401Ala
ENST00000693763.1:n.2313C>G
ENST00000245407.8:c.1153C>G MANE Select	ENSP00000245407.3:p.Pro385Ala
ENST00000245407.7:c.1153C>G	ENSP00000245407.3:p.Pro385Ala
ENST00000435065.6:c.1225C>G	ENSP00000402760.2:p.Pro409Ala
ENST00000447841.5:c.112-1643C>G
ENST00000448810.5:c.415C>G
ENST00000461013.5:n.8575C>G
ENST00000475308.1:n.1831C>G
ENST00000479605.5:n.256C>G
NM_001308122.1:c.1225C>G	NP_001295051.1:p.Pro409Ala
NM_003060.3:c.1153C>G	NP_003051.1:p.Pro385Ala
XM_011543590.1:c.535C>G	XP_011541892.1:p.Pro179Ala
XR_427718.1:n.1513C>G
XR_948290.1:n.1394-1643C>G
XR_948291.1:n.1507C>G
XM_011543590.2:c.535C>G	XP_011541892.1:p.Pro179Ala
XM_017009778.2:c.625C>G	XP_016865267.1:p.Pro209Ala
XR_001742215.1:n.1408C>G
XR_001742216.1:n.1427C>G
XR_427718.2:n.1513C>G
XR_948290.2:n.1394-1643C>G
XR_948291.2:n.1507C>G
NM_003060.4:c.1153C>G MANE Select	NP_003051.1:p.Pro385Ala
NM_001308122.2:c.1225C>G	NP_001295051.1:p.Pro409Ala