Canonical Allele Identifier: CA446339541

Gene: SLC22A5

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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