Canonical Allele Identifier: CA360807601

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131726465C>G (hg19) ; chr5:g.132390773C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132390773C>G , CM000667.2:g.132390773C>G	GRCh38
NC_000005.9:g.131726465C>G , CM000667.1:g.131726465C>G	GRCh37
NC_000005.8:g.131754364C>G	NCBI36
NG_008982.1:g.26065C>G
NG_008982.2:g.26070C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.977C>G	ENSP00000388838.2:p.Ser326Ter
ENST00000435065.7:c.1208C>G	ENSP00000402760.2:p.Ser403Ter
ENST00000448810.6:c.1053-3C>G	ENSP00000401860.2:n.1053-3C>G
ENST00000685543.1:n.1277C>G
ENST00000686757.1:c.*300C>G	ENSP00000510721.1:n.*300C>G
ENST00000687740.1:n.3821C>G
ENST00000688151.1:n.2446C>G
ENST00000689271.1:c.983C>G	ENSP00000510797.1:p.Ser328Ter
ENST00000690900.1:c.*300C>G	ENSP00000510703.1:n.*300C>G
ENST00000692212.1:n.2748C>G
ENST00000692355.1:c.389C>G
ENST00000692413.1:c.1118C>G	ENSP00000509374.1:p.Ser373Ter
ENST00000692825.1:c.1204C>G	ENSP00000509447.1:n.1204C>G
ENST00000693308.1:c.1184C>G	ENSP00000509770.1:p.Ser395Ter
ENST00000693763.1:n.2296C>G
ENST00000245407.8:c.1136C>G MANE Select	ENSP00000245407.3:p.Ser379Ter
ENST00000245407.7:c.1136C>G	ENSP00000245407.3:p.Ser379Ter
ENST00000435065.6:c.1208C>G	ENSP00000402760.2:p.Ser403Ter
ENST00000447841.5:c.112-1660C>G
ENST00000448810.5:c.401-3C>G
ENST00000461013.5:n.8558C>G
ENST00000475308.1:n.1814C>G
ENST00000479605.5:n.239C>G
NM_001308122.1:c.1208C>G	NP_001295051.1:p.Ser403Ter
NM_003060.3:c.1136C>G	NP_003051.1:p.Ser379Ter
XM_011543590.1:c.518C>G	XP_011541892.1:p.Ser173Ter
XR_427718.1:n.1496C>G
XR_948290.1:n.1394-1660C>G
XR_948291.1:n.1490C>G
XM_011543590.2:c.518C>G	XP_011541892.1:p.Ser173Ter
XM_017009778.2:c.608C>G	XP_016865267.1:p.Ser203Ter
XR_001742215.1:n.1394-3C>G
XR_001742216.1:n.1413-3C>G
XR_427718.2:n.1496C>G
XR_948290.2:n.1394-1660C>G
XR_948291.2:n.1490C>G
NM_003060.4:c.1136C>G MANE Select	NP_003051.1:p.Ser379Ter
NM_001308122.2:c.1208C>G	NP_001295051.1:p.Ser403Ter