Canonical Allele Identifier: CA360804683

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131719886G>A (hg19) ; chr5:g.132384194G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132384194G>A , CM000667.2:g.132384194G>A	GRCh38
NC_000005.9:g.131719886G>A , CM000667.1:g.131719886G>A	GRCh37
NC_000005.8:g.131747785G>A	NCBI36
NG_008982.1:g.19486G>A
NG_008982.2:g.19491G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.545G>A	ENSP00000388838.2:p.Gly182Asp
ENST00000435065.7:c.617G>A	ENSP00000402760.2:p.Gly206Asp
ENST00000448810.6:c.545G>A	ENSP00000401860.2:p.Gly182Asp
ENST00000686757.1:c.545G>A	ENSP00000510721.1:p.Gly182Asp
ENST00000687740.1:n.679G>A
ENST00000688151.1:n.1724G>A
ENST00000689271.1:c.545G>A	ENSP00000510797.1:p.Gly182Asp
ENST00000690900.1:c.545G>A	ENSP00000510703.1:p.Gly182Asp
ENST00000692355.1:c.97G>A
ENST00000692413.1:c.545G>A	ENSP00000509374.1:p.Gly182Asp
ENST00000692825.1:c.613G>A	ENSP00000509447.1:n.613G>A
ENST00000693308.1:c.545G>A	ENSP00000509770.1:p.Gly182Asp
ENST00000693763.1:n.679G>A
ENST00000245407.8:c.545G>A MANE Select	ENSP00000245407.3:p.Gly182Asp
ENST00000245407.7:c.545G>A	ENSP00000245407.3:p.Gly182Asp
ENST00000415928.5:c.314G>A	ENSP00000388838.1:p.Gly105Asp
ENST00000435065.6:c.617G>A	ENSP00000402760.2:p.Gly206Asp
ENST00000437841.6:c.394-1134G>A	ENSP00000400553.1:n.394-1134G>A
ENST00000461013.5:n.7967G>A
NM_001308122.1:c.617G>A	NP_001295051.1:p.Gly206Asp
NM_003060.3:c.545G>A	NP_003051.1:p.Gly182Asp
XM_011543590.1:c.-87G>A	XP_011541892.1:n.-87G>A
XR_427718.1:n.886G>A
XR_948290.1:n.886G>A
XR_948291.1:n.886G>A
XM_011543590.2:c.-87G>A	XP_011541892.1:n.-87G>A
XM_017009778.2:c.17G>A	XP_016865267.1:p.Gly6Asp
XR_001742215.1:n.886G>A
XR_001742216.1:n.886G>A
XR_427718.2:n.886G>A
XR_948290.2:n.886G>A
XR_948291.2:n.886G>A
NM_003060.4:c.545G>A MANE Select	NP_003051.1:p.Gly182Asp
NM_001308122.2:c.617G>A	NP_001295051.1:p.Gly206Asp