Canonical Allele Identifier: CA446339678

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131726541C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132390849C>G , CM000667.2:g.132390849C>G	GRCh38
NC_000005.9:g.131726541C>G , CM000667.1:g.131726541C>G	GRCh37
NC_000005.8:g.131754440C>G	NCBI36
NG_008982.1:g.26141C>G
NG_008982.2:g.26146C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.1053C>G	ENSP00000388838.2:p.Ala351=
ENST00000435065.7:c.1284C>G	ENSP00000402760.2:p.Ala428=
ENST00000448810.6:c.*64C>G	ENSP00000401860.2:n.*64C>G
ENST00000685543.1:n.1353C>G
ENST00000686757.1:c.*376C>G	ENSP00000510721.1:n.*376C>G
ENST00000687740.1:n.3897C>G
ENST00000688151.1:n.2522C>G
ENST00000689271.1:c.1059C>G	ENSP00000510797.1:p.Ala353=
ENST00000690900.1:c.*376C>G	ENSP00000510703.1:n.*376C>G
ENST00000692212.1:n.2824C>G
ENST00000692355.1:c.465C>G
ENST00000692413.1:c.1194C>G	ENSP00000509374.1:p.Ala398=
ENST00000692825.1:c.1280C>G	ENSP00000509447.1:n.1280C>G
ENST00000693308.1:c.1260C>G	ENSP00000509770.1:p.Ala420=
ENST00000693763.1:n.2372C>G
ENST00000245407.8:c.1212C>G MANE Select	ENSP00000245407.3:p.Ala404=
ENST00000245407.7:c.1212C>G	ENSP00000245407.3:p.Ala404=
ENST00000435065.6:c.1284C>G	ENSP00000402760.2:p.Ala428=
ENST00000447841.5:c.112-1584C>G
ENST00000448810.5:c.474C>G
ENST00000461013.5:n.8634C>G
ENST00000475308.1:n.1890C>G
ENST00000479605.5:n.315C>G
NM_001308122.1:c.1284C>G	NP_001295051.1:p.Ala428=
NM_003060.3:c.1212C>G	NP_003051.1:p.Ala404=
XM_011543590.1:c.594C>G	XP_011541892.1:p.Ala198=
XR_427718.1:n.1572C>G
XR_948290.1:n.1394-1584C>G
XR_948291.1:n.1566C>G
XM_011543590.2:c.594C>G	XP_011541892.1:p.Ala198=
XM_017009778.2:c.684C>G	XP_016865267.1:p.Ala228=
XR_001742215.1:n.1467C>G
XR_001742216.1:n.1486C>G
XR_427718.2:n.1572C>G
XR_948290.2:n.1394-1584C>G
XR_948291.2:n.1566C>G
NM_003060.4:c.1212C>G MANE Select	NP_003051.1:p.Ala404=
NM_001308122.2:c.1284C>G	NP_001295051.1:p.Ala428=