Canonical Allele Identifier: CA10622604
Gene: SLC22A5 HGNC NCBI
MIR3936HG HGNC NCBI

Linked Data

ClinVar Variation Id: 350808
dbSNP Id: rs538643468

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132369855G>A , CM000667.2:g.132369855G>A GRCh38
NC_000005.9:g.131705547G>A , CM000667.1:g.131705547G>A GRCh37
NC_000005.8:g.131733446G>A NCBI36
NG_008982.1:g.5147G>A
NG_008982.2:g.5152G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000415928.6:c.-118G>A (SLC22A5) ENSP00000388838.2:n.-118G>A
ENST00000435065.7:c.-118G>A (SLC22A5) ENSP00000402760.2:n.-118G>A
ENST00000448810.6:c.-118G>A (SLC22A5) ENSP00000401860.2:n.-118G>A
ENST00000686757.1:c.-118G>A (SLC22A5) ENSP00000510721.1:n.-118G>A
ENST00000687740.1:n.17G>A (SLC22A5)
ENST00000689271.1:c.-118G>A (SLC22A5) ENSP00000510797.1:n.-118G>A
ENST00000690900.1:c.-118G>A (SLC22A5) ENSP00000510703.1:n.-118G>A
ENST00000692413.1:c.-118G>A (SLC22A5) ENSP00000509374.1:n.-118G>A
ENST00000693308.1:c.-118G>A (SLC22A5) ENSP00000509770.1:n.-118G>A
ENST00000693763.1:n.17G>A (SLC22A5)
ENST00000245407.8:c.-118G>A (SLC22A5) MANE Select ENSP00000245407.3:n.-118G>A
ENST00000245407.7:c.-118G>A (SLC22A5) ENSP00000245407.3:n.-118G>A
NM_001308122.1:c.-118G>A (SLC22A5) NP_001295051.1:n.-118G>A
NM_003060.3:c.-118G>A (SLC22A5) NP_003051.1:n.-118G>A
NR_110997.1:n.62C>T (MIR3936HG)
XR_427718.1:n.152G>A (SLC22A5)
XR_948290.1:n.152G>A (SLC22A5)
XR_948291.1:n.152G>A (SLC22A5)
XR_001742215.1:n.152G>A (SLC22A5)
XR_001742216.1:n.152G>A (SLC22A5)
XR_427718.2:n.152G>A (SLC22A5)
XR_948290.2:n.152G>A (SLC22A5)
XR_948291.2:n.152G>A (SLC22A5)
NM_003060.4:c.-118G>A (SLC22A5) MANE Select NP_003051.1:n.-118G>A
NM_001308122.2:c.-118G>A (SLC22A5) NP_001295051.1:n.-118G>A