Canonical Allele Identifier: CA446339887

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131726559T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132390867T>C , CM000667.2:g.132390867T>C	GRCh38
NC_000005.9:g.131726559T>C , CM000667.1:g.131726559T>C	GRCh37
NC_000005.8:g.131754458T>C	NCBI36
NG_008982.1:g.26159T>C
NG_008982.2:g.26164T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.1071T>C	ENSP00000388838.2:p.Gly357=
ENST00000435065.7:c.1302T>C	ENSP00000402760.2:p.Gly434=
ENST00000448810.6:c.*82T>C	ENSP00000401860.2:n.*82T>C
ENST00000685543.1:n.1371T>C
ENST00000686757.1:c.*394T>C	ENSP00000510721.1:n.*394T>C
ENST00000687740.1:n.3915T>C
ENST00000688151.1:n.2540T>C
ENST00000689271.1:c.1077T>C	ENSP00000510797.1:p.Gly359=
ENST00000690900.1:c.*394T>C	ENSP00000510703.1:n.*394T>C
ENST00000692212.1:n.2842T>C
ENST00000692355.1:c.483T>C
ENST00000692413.1:c.1212T>C	ENSP00000509374.1:p.Gly404=
ENST00000692825.1:c.1298T>C	ENSP00000509447.1:n.1298T>C
ENST00000693308.1:c.1278T>C	ENSP00000509770.1:p.Gly426=
ENST00000693763.1:n.2390T>C
ENST00000245407.8:c.1230T>C MANE Select	ENSP00000245407.3:p.Gly410=
ENST00000245407.7:c.1230T>C	ENSP00000245407.3:p.Gly410=
ENST00000435065.6:c.1302T>C	ENSP00000402760.2:p.Gly434=
ENST00000447841.5:c.112-1566T>C
ENST00000448810.5:c.492T>C
ENST00000461013.5:n.8652T>C
ENST00000475308.1:n.1908T>C
ENST00000479605.5:n.333T>C
NM_001308122.1:c.1302T>C	NP_001295051.1:p.Gly434=
NM_003060.3:c.1230T>C	NP_003051.1:p.Gly410=
XM_011543590.1:c.612T>C	XP_011541892.1:p.Gly204=
XR_427718.1:n.1590T>C
XR_948290.1:n.1394-1566T>C
XR_948291.1:n.1584T>C
XM_011543590.2:c.612T>C	XP_011541892.1:p.Gly204=
XM_017009778.2:c.702T>C	XP_016865267.1:p.Gly234=
XR_001742215.1:n.1485T>C
XR_001742216.1:n.1504T>C
XR_427718.2:n.1590T>C
XR_948290.2:n.1394-1566T>C
XR_948291.2:n.1584T>C
NM_003060.4:c.1230T>C MANE Select	NP_003051.1:p.Gly410=
NM_001308122.2:c.1302T>C	NP_001295051.1:p.Gly434=