Canonical Allele Identifier: CA446330472

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131721174A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132385482A>C , CM000667.2:g.132385482A>C	GRCh38
NC_000005.9:g.131721174A>C , CM000667.1:g.131721174A>C	GRCh37
NC_000005.8:g.131749073A>C	NCBI36
NG_008982.1:g.20774A>C
NG_008982.2:g.20779A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.665+1168A>C	ENSP00000388838.2:n.665+1168A>C
ENST00000435065.7:c.879A>C	ENSP00000402760.2:p.Leu293=
ENST00000448810.6:c.807A>C	ENSP00000401860.2:p.Leu269=
ENST00000686757.1:c.826A>C	ENSP00000510721.1:p.Met276Leu
ENST00000687740.1:n.1967A>C
ENST00000688151.1:n.1999A>C
ENST00000689271.1:c.671+1162A>C	ENSP00000510797.1:n.671+1162A>C
ENST00000690900.1:c.778A>C	ENSP00000510703.1:p.Met260Leu
ENST00000692212.1:n.633A>C
ENST00000692355.1:c.204+1181A>C
ENST00000692413.1:c.826A>C	ENSP00000509374.1:p.Met276Leu
ENST00000692825.1:c.875A>C	ENSP00000509447.1:n.875A>C
ENST00000693308.1:c.820A>C	ENSP00000509770.1:p.Met274Leu
ENST00000693763.1:n.1967A>C
ENST00000245407.8:c.807A>C MANE Select	ENSP00000245407.3:p.Leu269=
ENST00000245407.7:c.807A>C	ENSP00000245407.3:p.Leu269=
ENST00000415928.5:c.576A>C	ENSP00000388838.1:p.Leu192=
ENST00000435065.6:c.879A>C	ENSP00000402760.2:p.Leu293=
ENST00000437841.6:c.*122A>C	ENSP00000400553.1:n.*122A>C
ENST00000448810.5:c.155A>C
ENST00000461013.5:n.8229A>C
NM_001308122.1:c.879A>C	NP_001295051.1:p.Leu293=
NM_003060.3:c.807A>C	NP_003051.1:p.Leu269=
XM_011543590.1:c.189A>C	XP_011541892.1:p.Leu63=
XR_427718.1:n.1167A>C
XR_948290.1:n.1148A>C
XR_948291.1:n.1161A>C
XM_011543590.2:c.189A>C	XP_011541892.1:p.Leu63=
XM_017009778.2:c.279A>C	XP_016865267.1:p.Leu93=
XR_001742215.1:n.1148A>C
XR_001742216.1:n.1167A>C
XR_427718.2:n.1167A>C
XR_948290.2:n.1148A>C
XR_948291.2:n.1161A>C
NM_003060.4:c.807A>C MANE Select	NP_003051.1:p.Leu269=
NM_001308122.2:c.879A>C	NP_001295051.1:p.Leu293=