Canonical Allele Identifier: CA446342938

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131728183C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132392491C>G , CM000667.2:g.132392491C>G	GRCh38
NC_000005.9:g.131728183C>G , CM000667.1:g.131728183C>G	GRCh37
NC_000005.8:g.131756082C>G	NCBI36
NG_008982.1:g.27783C>G
NG_008982.2:g.27788C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000415928.6:c.1167C>G	ENSP00000388838.2:p.Ala389=
ENST00000435065.7:c.1398C>G	ENSP00000402760.2:p.Ala466=
ENST00000448810.6:c.*178C>G	ENSP00000401860.2:n.*178C>G
ENST00000685543.1:n.1467C>G
ENST00000686757.1:c.*490C>G	ENSP00000510721.1:n.*490C>G
ENST00000687740.1:n.4011C>G
ENST00000688151.1:n.2636C>G
ENST00000689271.1:c.1173C>G	ENSP00000510797.1:p.Ala391=
ENST00000690900.1:c.*490C>G	ENSP00000510703.1:n.*490C>G
ENST00000692212.1:n.4466C>G
ENST00000692355.1:c.579C>G
ENST00000692413.1:c.1308C>G	ENSP00000509374.1:p.Ala436=
ENST00000692825.1:c.1394C>G	ENSP00000509447.1:n.1394C>G
ENST00000693308.1:c.1374C>G	ENSP00000509770.1:p.Ala458=
ENST00000693763.1:n.2486C>G
ENST00000245407.8:c.1326C>G MANE Select	ENSP00000245407.3:p.Ala442=
ENST00000245407.7:c.1326C>G	ENSP00000245407.3:p.Ala442=
ENST00000435065.6:c.1398C>G	ENSP00000402760.2:p.Ala466=
ENST00000447841.5:c.170C>G
ENST00000448810.5:c.588C>G
ENST00000461013.5:n.8748C>G
ENST00000475308.1:n.2004C>G
ENST00000479605.5:n.429C>G
NM_001308122.1:c.1398C>G	NP_001295051.1:p.Ala466=
NM_003060.3:c.1326C>G	NP_003051.1:p.Ala442=
XM_011543590.1:c.708C>G	XP_011541892.1:p.Ala236=
XR_948290.1:n.1452C>G
XM_011543590.2:c.708C>G	XP_011541892.1:p.Ala236=
XM_017009778.2:c.798C>G	XP_016865267.1:p.Ala266=
XR_001742215.1:n.1581C>G
XR_001742216.1:n.1600C>G
XR_427718.2:n.1686C>G
XR_948290.2:n.1452C>G
XR_948291.2:n.1680C>G
NM_003060.4:c.1326C>G MANE Select	NP_003051.1:p.Ala442=
NM_001308122.2:c.1398C>G	NP_001295051.1:p.Ala466=