Canonical Allele Identifier: CA446342992

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131728189C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132392497C>G , CM000667.2:g.132392497C>G	GRCh38
NC_000005.9:g.131728189C>G , CM000667.1:g.131728189C>G	GRCh37
NC_000005.8:g.131756088C>G	NCBI36
NG_008982.1:g.27789C>G
NG_008982.2:g.27794C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000415928.6:c.1173C>G	ENSP00000388838.2:p.Ser391=
ENST00000435065.7:c.1404C>G	ENSP00000402760.2:p.Ser468=
ENST00000448810.6:c.*184C>G	ENSP00000401860.2:n.*184C>G
ENST00000685543.1:n.1473C>G
ENST00000686757.1:c.*496C>G	ENSP00000510721.1:n.*496C>G
ENST00000687740.1:n.4017C>G
ENST00000688151.1:n.2642C>G
ENST00000689271.1:c.1179C>G	ENSP00000510797.1:p.Ser393=
ENST00000690900.1:c.*496C>G	ENSP00000510703.1:n.*496C>G
ENST00000692212.1:n.4472C>G
ENST00000692355.1:c.585C>G
ENST00000692413.1:c.1314C>G	ENSP00000509374.1:p.Ser438=
ENST00000692825.1:c.1400C>G	ENSP00000509447.1:n.1400C>G
ENST00000693308.1:c.1380C>G	ENSP00000509770.1:p.Ser460=
ENST00000693763.1:n.2492C>G
ENST00000245407.8:c.1332C>G MANE Select	ENSP00000245407.3:p.Ser444=
ENST00000245407.7:c.1332C>G	ENSP00000245407.3:p.Ser444=
ENST00000435065.6:c.1404C>G	ENSP00000402760.2:p.Ser468=
ENST00000447841.5:c.176C>G
ENST00000448810.5:c.594C>G
ENST00000461013.5:n.8754C>G
ENST00000475308.1:n.2010C>G
ENST00000479605.5:n.435C>G
NM_001308122.1:c.1404C>G	NP_001295051.1:p.Ser468=
NM_003060.3:c.1332C>G	NP_003051.1:p.Ser444=
XM_011543590.1:c.714C>G	XP_011541892.1:p.Ser238=
XR_948290.1:n.1458C>G
XM_011543590.2:c.714C>G	XP_011541892.1:p.Ser238=
XM_017009778.2:c.804C>G	XP_016865267.1:p.Ser268=
XR_001742215.1:n.1587C>G
XR_001742216.1:n.1606C>G
XR_427718.2:n.1692C>G
XR_948290.2:n.1458C>G
XR_948291.2:n.1686C>G
NM_003060.4:c.1332C>G MANE Select	NP_003051.1:p.Ser444=
NM_001308122.2:c.1404C>G	NP_001295051.1:p.Ser468=