Canonical Allele Identifier: CA446346188

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131729432C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132393740C>G , CM000667.2:g.132393740C>G	GRCh38
NC_000005.9:g.131729432C>G , CM000667.1:g.131729432C>G	GRCh37
NC_000005.8:g.131757331C>G	NCBI36
NG_008982.1:g.29032C>G
NG_008982.2:g.29037C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.1292-445C>G	ENSP00000388838.2:n.1292-445C>G
ENST00000435065.7:c.1587C>G	ENSP00000402760.2:p.Leu529=
ENST00000448810.6:c.*367C>G	ENSP00000401860.2:n.*367C>G
ENST00000685543.1:n.1656C>G
ENST00000686757.1:c.*679C>G	ENSP00000510721.1:n.*679C>G
ENST00000686868.1:n.507C>G
ENST00000687740.1:n.4200C>G
ENST00000688151.1:n.2825C>G
ENST00000689271.1:c.1362C>G	ENSP00000510797.1:p.Leu454=
ENST00000690900.1:c.*679C>G	ENSP00000510703.1:n.*679C>G
ENST00000692212.1:n.4655C>G
ENST00000692355.1:c.768C>G
ENST00000692413.1:c.1497C>G	ENSP00000509374.1:p.Leu499=
ENST00000692825.1:c.1583C>G	ENSP00000509447.1:n.1583C>G
ENST00000693308.1:c.1563C>G	ENSP00000509770.1:p.Leu521=
ENST00000693763.1:n.2675C>G
ENST00000245407.8:c.1515C>G MANE Select	ENSP00000245407.3:p.Leu505=
ENST00000245407.7:c.1515C>G	ENSP00000245407.3:p.Leu505=
ENST00000435065.6:c.1587C>G	ENSP00000402760.2:p.Leu529=
ENST00000447841.5:c.359C>G
ENST00000448810.5:c.777C>G
ENST00000461013.5:n.8937C>G
ENST00000475308.1:n.2193C>G
NM_001308122.1:c.1587C>G	NP_001295051.1:p.Leu529=
NM_003060.3:c.1515C>G	NP_003051.1:p.Leu505=
XM_011543590.1:c.897C>G	XP_011541892.1:p.Leu299=
XR_948290.1:n.1641C>G
XM_011543590.2:c.897C>G	XP_011541892.1:p.Leu299=
XM_017009778.2:c.987C>G	XP_016865267.1:p.Leu329=
XR_001742215.1:n.1770C>G
XR_001742216.1:n.1789C>G
XR_427718.2:n.1875C>G
XR_948290.2:n.1641C>G
XR_948291.2:n.1869C>G
NM_003060.4:c.1515C>G MANE Select	NP_003051.1:p.Leu505=
NM_001308122.2:c.1587C>G	NP_001295051.1:p.Leu529=