Canonical Allele Identifier: CA446339544

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131726529C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132390837C>G , CM000667.2:g.132390837C>G	GRCh38
NC_000005.9:g.131726529C>G , CM000667.1:g.131726529C>G	GRCh37
NC_000005.8:g.131754428C>G	NCBI36
NG_008982.1:g.26129C>G
NG_008982.2:g.26134C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.1041C>G	ENSP00000388838.2:p.Arg347=
ENST00000435065.7:c.1272C>G	ENSP00000402760.2:p.Arg424=
ENST00000448810.6:c.*52C>G	ENSP00000401860.2:n.*52C>G
ENST00000685543.1:n.1341C>G
ENST00000686757.1:c.*364C>G	ENSP00000510721.1:n.*364C>G
ENST00000687740.1:n.3885C>G
ENST00000688151.1:n.2510C>G
ENST00000689271.1:c.1047C>G	ENSP00000510797.1:p.Arg349=
ENST00000690900.1:c.*364C>G	ENSP00000510703.1:n.*364C>G
ENST00000692212.1:n.2812C>G
ENST00000692355.1:c.453C>G
ENST00000692413.1:c.1182C>G	ENSP00000509374.1:p.Arg394=
ENST00000692825.1:c.1268C>G	ENSP00000509447.1:n.1268C>G
ENST00000693308.1:c.1248C>G	ENSP00000509770.1:p.Arg416=
ENST00000693763.1:n.2360C>G
ENST00000245407.8:c.1200C>G MANE Select	ENSP00000245407.3:p.Arg400=
ENST00000245407.7:c.1200C>G	ENSP00000245407.3:p.Arg400=
ENST00000435065.6:c.1272C>G	ENSP00000402760.2:p.Arg424=
ENST00000447841.5:c.112-1596C>G
ENST00000448810.5:c.462C>G
ENST00000461013.5:n.8622C>G
ENST00000475308.1:n.1878C>G
ENST00000479605.5:n.303C>G
NM_001308122.1:c.1272C>G	NP_001295051.1:p.Arg424=
NM_003060.3:c.1200C>G	NP_003051.1:p.Arg400=
XM_011543590.1:c.582C>G	XP_011541892.1:p.Arg194=
XR_427718.1:n.1560C>G
XR_948290.1:n.1394-1596C>G
XR_948291.1:n.1554C>G
XM_011543590.2:c.582C>G	XP_011541892.1:p.Arg194=
XM_017009778.2:c.672C>G	XP_016865267.1:p.Arg224=
XR_001742215.1:n.1455C>G
XR_001742216.1:n.1474C>G
XR_427718.2:n.1560C>G
XR_948290.2:n.1394-1596C>G
XR_948291.2:n.1554C>G
NM_003060.4:c.1200C>G MANE Select	NP_003051.1:p.Arg400=
NM_001308122.2:c.1272C>G	NP_001295051.1:p.Arg424=