Canonical Allele Identifier: CA360807645

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131726486C>G (hg19) ; chr5:g.132390794C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132390794C>G , CM000667.2:g.132390794C>G	GRCh38
NC_000005.9:g.131726486C>G , CM000667.1:g.131726486C>G	GRCh37
NC_000005.8:g.131754385C>G	NCBI36
NG_008982.1:g.26086C>G
NG_008982.2:g.26091C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.998C>G	ENSP00000388838.2:p.Ala333Gly
ENST00000435065.7:c.1229C>G	ENSP00000402760.2:p.Ala410Gly
ENST00000448810.6:c.*9C>G	ENSP00000401860.2:n.*9C>G
ENST00000685543.1:n.1298C>G
ENST00000686757.1:c.*321C>G	ENSP00000510721.1:n.*321C>G
ENST00000687740.1:n.3842C>G
ENST00000688151.1:n.2467C>G
ENST00000689271.1:c.1004C>G	ENSP00000510797.1:p.Ala335Gly
ENST00000690900.1:c.*321C>G	ENSP00000510703.1:n.*321C>G
ENST00000692212.1:n.2769C>G
ENST00000692355.1:c.410C>G
ENST00000692413.1:c.1139C>G	ENSP00000509374.1:p.Ala380Gly
ENST00000692825.1:c.1225C>G	ENSP00000509447.1:n.1225C>G
ENST00000693308.1:c.1205C>G	ENSP00000509770.1:p.Ala402Gly
ENST00000693763.1:n.2317C>G
ENST00000245407.8:c.1157C>G MANE Select	ENSP00000245407.3:p.Ala386Gly
ENST00000245407.7:c.1157C>G	ENSP00000245407.3:p.Ala386Gly
ENST00000435065.6:c.1229C>G	ENSP00000402760.2:p.Ala410Gly
ENST00000447841.5:c.112-1639C>G
ENST00000448810.5:c.419C>G
ENST00000461013.5:n.8579C>G
ENST00000475308.1:n.1835C>G
ENST00000479605.5:n.260C>G
NM_001308122.1:c.1229C>G	NP_001295051.1:p.Ala410Gly
NM_003060.3:c.1157C>G	NP_003051.1:p.Ala386Gly
XM_011543590.1:c.539C>G	XP_011541892.1:p.Ala180Gly
XR_427718.1:n.1517C>G
XR_948290.1:n.1394-1639C>G
XR_948291.1:n.1511C>G
XM_011543590.2:c.539C>G	XP_011541892.1:p.Ala180Gly
XM_017009778.2:c.629C>G	XP_016865267.1:p.Ala210Gly
XR_001742215.1:n.1412C>G
XR_001742216.1:n.1431C>G
XR_427718.2:n.1517C>G
XR_948290.2:n.1394-1639C>G
XR_948291.2:n.1511C>G
NM_003060.4:c.1157C>G MANE Select	NP_003051.1:p.Ala386Gly
NM_001308122.2:c.1229C>G	NP_001295051.1:p.Ala410Gly