Canonical Allele Identifier: CA446337695

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131726424T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132390732T>C , CM000667.2:g.132390732T>C	GRCh38
NC_000005.9:g.131726424T>C , CM000667.1:g.131726424T>C	GRCh37
NC_000005.8:g.131754323T>C	NCBI36
NG_008982.1:g.26024T>C
NG_008982.2:g.26029T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000415928.6:c.936T>C	ENSP00000388838.2:p.Thr312=
ENST00000435065.7:c.1167T>C	ENSP00000402760.2:p.Thr389=
ENST00000448810.6:c.1053-44T>C	ENSP00000401860.2:n.1053-44T>C
ENST00000685543.1:n.1236T>C
ENST00000686757.1:c.*259T>C	ENSP00000510721.1:n.*259T>C
ENST00000687740.1:n.3780T>C
ENST00000688151.1:n.2405T>C
ENST00000689271.1:c.942T>C	ENSP00000510797.1:p.Thr314=
ENST00000690900.1:c.*259T>C	ENSP00000510703.1:n.*259T>C
ENST00000692212.1:n.2707T>C
ENST00000692355.1:c.348T>C
ENST00000692413.1:c.1077T>C	ENSP00000509374.1:p.Thr359=
ENST00000692825.1:c.1163T>C	ENSP00000509447.1:n.1163T>C
ENST00000693308.1:c.1143T>C	ENSP00000509770.1:p.Thr381=
ENST00000693763.1:n.2255T>C
ENST00000245407.8:c.1095T>C MANE Select	ENSP00000245407.3:p.Thr365=
ENST00000245407.7:c.1095T>C	ENSP00000245407.3:p.Thr365=
ENST00000435065.6:c.1167T>C	ENSP00000402760.2:p.Thr389=
ENST00000447841.5:c.112-1701T>C
ENST00000448810.5:c.401-44T>C
ENST00000461013.5:n.8517T>C
ENST00000475308.1:n.1773T>C
ENST00000479605.5:n.198T>C
NM_001308122.1:c.1167T>C	NP_001295051.1:p.Thr389=
NM_003060.3:c.1095T>C	NP_003051.1:p.Thr365=
XM_011543590.1:c.477T>C	XP_011541892.1:p.Thr159=
XR_427718.1:n.1455T>C
XR_948290.1:n.1394-1701T>C
XR_948291.1:n.1449T>C
XM_011543590.2:c.477T>C	XP_011541892.1:p.Thr159=
XM_017009778.2:c.567T>C	XP_016865267.1:p.Thr189=
XR_001742215.1:n.1394-44T>C
XR_001742216.1:n.1413-44T>C
XR_427718.2:n.1455T>C
XR_948290.2:n.1394-1701T>C
XR_948291.2:n.1449T>C
NM_003060.4:c.1095T>C MANE Select	NP_003051.1:p.Thr365=
NM_001308122.2:c.1167T>C	NP_001295051.1:p.Thr389=