Canonical Allele Identifier: CA446330343

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131721153G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132385461G>T , CM000667.2:g.132385461G>T	GRCh38
NC_000005.9:g.131721153G>T , CM000667.1:g.131721153G>T	GRCh37
NC_000005.8:g.131749052G>T	NCBI36
NG_008982.1:g.20753G>T
NG_008982.2:g.20758G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.665+1147G>T	ENSP00000388838.2:n.665+1147G>T
ENST00000435065.7:c.858G>T	ENSP00000402760.2:p.Ala286=
ENST00000448810.6:c.786G>T	ENSP00000401860.2:p.Ala262=
ENST00000686757.1:c.805G>T	ENSP00000510721.1:p.Ala269Ser
ENST00000687740.1:n.1946G>T
ENST00000688151.1:n.1978G>T
ENST00000689271.1:c.671+1141G>T	ENSP00000510797.1:n.671+1141G>T
ENST00000690900.1:c.757G>T	ENSP00000510703.1:p.Ala253Ser
ENST00000692212.1:n.612G>T
ENST00000692355.1:c.204+1160G>T
ENST00000692413.1:c.805G>T	ENSP00000509374.1:p.Ala269Ser
ENST00000692825.1:c.854G>T	ENSP00000509447.1:n.854G>T
ENST00000693308.1:c.799G>T	ENSP00000509770.1:p.Ala267Ser
ENST00000693763.1:n.1946G>T
ENST00000245407.8:c.786G>T MANE Select	ENSP00000245407.3:p.Ala262=
ENST00000245407.7:c.786G>T	ENSP00000245407.3:p.Ala262=
ENST00000415928.5:c.555G>T	ENSP00000388838.1:p.Ala185=
ENST00000435065.6:c.858G>T	ENSP00000402760.2:p.Ala286=
ENST00000437841.6:c.*101G>T	ENSP00000400553.1:n.*101G>T
ENST00000448810.5:c.134G>T
ENST00000461013.5:n.8208G>T
NM_001308122.1:c.858G>T	NP_001295051.1:p.Ala286=
NM_003060.3:c.786G>T	NP_003051.1:p.Ala262=
XM_011543590.1:c.168G>T	XP_011541892.1:p.Ala56=
XR_427718.1:n.1146G>T
XR_948290.1:n.1127G>T
XR_948291.1:n.1140G>T
XM_011543590.2:c.168G>T	XP_011541892.1:p.Ala56=
XM_017009778.2:c.258G>T	XP_016865267.1:p.Ala86=
XR_001742215.1:n.1127G>T
XR_001742216.1:n.1146G>T
XR_427718.2:n.1146G>T
XR_948290.2:n.1127G>T
XR_948291.2:n.1140G>T
NM_003060.4:c.786G>T MANE Select	NP_003051.1:p.Ala262=
NM_001308122.2:c.858G>T	NP_001295051.1:p.Ala286=