Canonical Allele Identifier: CA446337309

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131726388C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132390696C>G , CM000667.2:g.132390696C>G	GRCh38
NC_000005.9:g.131726388C>G , CM000667.1:g.131726388C>G	GRCh37
NC_000005.8:g.131754287C>G	NCBI36
NG_008982.1:g.25988C>G
NG_008982.2:g.25993C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.900C>G	ENSP00000388838.2:p.Thr300=
ENST00000435065.7:c.1131C>G	ENSP00000402760.2:p.Thr377=
ENST00000448810.6:c.1053-80C>G	ENSP00000401860.2:n.1053-80C>G
ENST00000685543.1:n.1200C>G
ENST00000686757.1:c.*223C>G	ENSP00000510721.1:n.*223C>G
ENST00000687740.1:n.3744C>G
ENST00000688151.1:n.2369C>G
ENST00000689271.1:c.906C>G	ENSP00000510797.1:p.Thr302=
ENST00000690900.1:c.*223C>G	ENSP00000510703.1:n.*223C>G
ENST00000692212.1:n.2671C>G
ENST00000692355.1:c.312C>G
ENST00000692413.1:c.1041C>G	ENSP00000509374.1:p.Thr347=
ENST00000692825.1:c.1127C>G	ENSP00000509447.1:n.1127C>G
ENST00000693308.1:c.1107C>G	ENSP00000509770.1:p.Thr369=
ENST00000693763.1:n.2219C>G
ENST00000245407.8:c.1059C>G MANE Select	ENSP00000245407.3:p.Thr353=
ENST00000245407.7:c.1059C>G	ENSP00000245407.3:p.Thr353=
ENST00000435065.6:c.1131C>G	ENSP00000402760.2:p.Thr377=
ENST00000447841.5:c.111+1675C>G
ENST00000448810.5:c.401-80C>G
ENST00000461013.5:n.8481C>G
ENST00000475308.1:n.1737C>G
ENST00000479605.5:n.162C>G
NM_001308122.1:c.1131C>G	NP_001295051.1:p.Thr377=
NM_003060.3:c.1059C>G	NP_003051.1:p.Thr353=
XM_011543590.1:c.441C>G	XP_011541892.1:p.Thr147=
XR_427718.1:n.1419C>G
XR_948290.1:n.1393+1675C>G
XR_948291.1:n.1413C>G
XM_011543590.2:c.441C>G	XP_011541892.1:p.Thr147=
XM_017009778.2:c.531C>G	XP_016865267.1:p.Thr177=
XR_001742215.1:n.1394-80C>G
XR_001742216.1:n.1413-80C>G
XR_427718.2:n.1419C>G
XR_948290.2:n.1393+1675C>G
XR_948291.2:n.1413C>G
NM_003060.4:c.1059C>G MANE Select	NP_003051.1:p.Thr353=
NM_001308122.2:c.1131C>G	NP_001295051.1:p.Thr377=