Canonical Allele Identifier: CA446327986

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131714084T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132378392T>C , CM000667.2:g.132378392T>C	GRCh38
NC_000005.9:g.131714084T>C , CM000667.1:g.131714084T>C	GRCh37
NC_000005.8:g.131741983T>C	NCBI36
NG_008982.1:g.13684T>C
NG_008982.2:g.13689T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000415928.6:c.408T>C	ENSP00000388838.2:p.Cys136=
ENST00000435065.7:c.480T>C	ENSP00000402760.2:p.Cys160=
ENST00000448810.6:c.408T>C	ENSP00000401860.2:p.Cys136=
ENST00000686757.1:c.408T>C	ENSP00000510721.1:p.Cys136=
ENST00000687740.1:n.542T>C
ENST00000689271.1:c.408T>C	ENSP00000510797.1:p.Cys136=
ENST00000690900.1:c.408T>C	ENSP00000510703.1:p.Cys136=
ENST00000692413.1:c.408T>C	ENSP00000509374.1:p.Cys136=
ENST00000692825.1:c.476T>C	ENSP00000509447.1:n.476T>C
ENST00000693308.1:c.408T>C	ENSP00000509770.1:p.Cys136=
ENST00000693763.1:n.542T>C
ENST00000245407.8:c.408T>C MANE Select	ENSP00000245407.3:p.Cys136=
ENST00000245407.7:c.408T>C	ENSP00000245407.3:p.Cys136=
ENST00000415928.5:c.177T>C	ENSP00000388838.1:p.Cys59=
ENST00000435065.6:c.480T>C	ENSP00000402760.2:p.Cys160=
ENST00000437841.6:c.394-6936T>C	ENSP00000400553.1:n.394-6936T>C
ENST00000461013.5:n.2165T>C
NM_001308122.1:c.480T>C	NP_001295051.1:p.Cys160=
NM_003060.3:c.408T>C	NP_003051.1:p.Cys136=
XR_427718.1:n.749T>C
XR_948290.1:n.749T>C
XR_948291.1:n.749T>C
XM_011543590.2:c.-224T>C	XP_011541892.1:n.-224T>C
XM_017009778.2:c.-31-5755T>C	XP_016865267.1:n.-31-5755T>C
XR_001742215.1:n.749T>C
XR_001742216.1:n.749T>C
XR_427718.2:n.749T>C
XR_948290.2:n.749T>C
XR_948291.2:n.749T>C
NM_003060.4:c.408T>C MANE Select	NP_003051.1:p.Cys136=
NM_001308122.2:c.480T>C	NP_001295051.1:p.Cys160=