Canonical Allele Identifier: CA360807395

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131726392T>A (hg19) ; chr5:g.132390700T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132390700T>A , CM000667.2:g.132390700T>A	GRCh38
NC_000005.9:g.131726392T>A , CM000667.1:g.131726392T>A	GRCh37
NC_000005.8:g.131754291T>A	NCBI36
NG_008982.1:g.25992T>A
NG_008982.2:g.25997T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.904T>A	ENSP00000388838.2:p.Ser302Thr
ENST00000435065.7:c.1135T>A	ENSP00000402760.2:p.Ser379Thr
ENST00000448810.6:c.1053-76T>A	ENSP00000401860.2:n.1053-76T>A
ENST00000685543.1:n.1204T>A
ENST00000686757.1:c.*227T>A	ENSP00000510721.1:n.*227T>A
ENST00000687740.1:n.3748T>A
ENST00000688151.1:n.2373T>A
ENST00000689271.1:c.910T>A	ENSP00000510797.1:p.Ser304Thr
ENST00000690900.1:c.*227T>A	ENSP00000510703.1:n.*227T>A
ENST00000692212.1:n.2675T>A
ENST00000692355.1:c.316T>A
ENST00000692413.1:c.1045T>A	ENSP00000509374.1:p.Ser349Thr
ENST00000692825.1:c.1131T>A	ENSP00000509447.1:n.1131T>A
ENST00000693308.1:c.1111T>A	ENSP00000509770.1:p.Ser371Thr
ENST00000693763.1:n.2223T>A
ENST00000245407.8:c.1063T>A MANE Select	ENSP00000245407.3:p.Ser355Thr
ENST00000245407.7:c.1063T>A	ENSP00000245407.3:p.Ser355Thr
ENST00000435065.6:c.1135T>A	ENSP00000402760.2:p.Ser379Thr
ENST00000447841.5:c.111+1679T>A
ENST00000448810.5:c.401-76T>A
ENST00000461013.5:n.8485T>A
ENST00000475308.1:n.1741T>A
ENST00000479605.5:n.166T>A
NM_001308122.1:c.1135T>A	NP_001295051.1:p.Ser379Thr
NM_003060.3:c.1063T>A	NP_003051.1:p.Ser355Thr
XM_011543590.1:c.445T>A	XP_011541892.1:p.Ser149Thr
XR_427718.1:n.1423T>A
XR_948290.1:n.1393+1679T>A
XR_948291.1:n.1417T>A
XM_011543590.2:c.445T>A	XP_011541892.1:p.Ser149Thr
XM_017009778.2:c.535T>A	XP_016865267.1:p.Ser179Thr
XR_001742215.1:n.1394-76T>A
XR_001742216.1:n.1413-76T>A
XR_427718.2:n.1423T>A
XR_948290.2:n.1393+1679T>A
XR_948291.2:n.1417T>A
NM_003060.4:c.1063T>A MANE Select	NP_003051.1:p.Ser355Thr
NM_001308122.2:c.1135T>A	NP_001295051.1:p.Ser379Thr