Canonical Allele Identifier: CA360807602

Gene: SLC22A5

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.977C>T	ENSP00000388838.2:p.Ser326Leu
ENST00000435065.7:c.1208C>T	ENSP00000402760.2:p.Ser403Leu
ENST00000448810.6:c.1053-3C>T	ENSP00000401860.2:n.1053-3C>T
ENST00000685543.1:n.1277C>T
ENST00000686757.1:c.*300C>T	ENSP00000510721.1:n.*300C>T
ENST00000687740.1:n.3821C>T
ENST00000688151.1:n.2446C>T
ENST00000689271.1:c.983C>T	ENSP00000510797.1:p.Ser328Leu
ENST00000690900.1:c.*300C>T	ENSP00000510703.1:n.*300C>T
ENST00000692212.1:n.2748C>T
ENST00000692355.1:c.389C>T
ENST00000692413.1:c.1118C>T	ENSP00000509374.1:p.Ser373Leu
ENST00000692825.1:c.1204C>T	ENSP00000509447.1:n.1204C>T
ENST00000693308.1:c.1184C>T	ENSP00000509770.1:p.Ser395Leu
ENST00000693763.1:n.2296C>T
ENST00000245407.8:c.1136C>T MANE Select	ENSP00000245407.3:p.Ser379Leu
ENST00000245407.7:c.1136C>T	ENSP00000245407.3:p.Ser379Leu
ENST00000435065.6:c.1208C>T	ENSP00000402760.2:p.Ser403Leu
ENST00000447841.5:c.112-1660C>T
ENST00000448810.5:c.401-3C>T
ENST00000461013.5:n.8558C>T
ENST00000475308.1:n.1814C>T
ENST00000479605.5:n.239C>T
NM_001308122.1:c.1208C>T	NP_001295051.1:p.Ser403Leu
NM_003060.3:c.1136C>T	NP_003051.1:p.Ser379Leu
XM_011543590.1:c.518C>T	XP_011541892.1:p.Ser173Leu
XR_427718.1:n.1496C>T
XR_948290.1:n.1394-1660C>T
XR_948291.1:n.1490C>T
XM_011543590.2:c.518C>T	XP_011541892.1:p.Ser173Leu
XM_017009778.2:c.608C>T	XP_016865267.1:p.Ser203Leu
XR_001742215.1:n.1394-3C>T
XR_001742216.1:n.1413-3C>T
XR_427718.2:n.1496C>T
XR_948290.2:n.1394-1660C>T
XR_948291.2:n.1490C>T
NM_003060.4:c.1136C>T MANE Select	NP_003051.1:p.Ser379Leu
NM_001308122.2:c.1208C>T	NP_001295051.1:p.Ser403Leu