Canonical Allele Identifier: CA3404064
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1618373
ClinVar RCV Id: RCV002082029
dbSNP Id: rs372778184

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132390671C>A , CM000667.2:g.132390671C>A GRCh38
NC_000005.9:g.131726363C>A , CM000667.1:g.131726363C>A GRCh37
NC_000005.8:g.131754262C>A NCBI36
NG_008982.1:g.25963C>A
NG_008982.2:g.25968C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000415928.6:c.894-19C>A ENSP00000388838.2:n.894-19C>A
ENST00000435065.7:c.1125-19C>A ENSP00000402760.2:n.1125-19C>A
ENST00000448810.6:c.1053-105C>A ENSP00000401860.2:n.1053-105C>A
ENST00000685543.1:n.1194-19C>A
ENST00000686757.1:c.*217-19C>A ENSP00000510721.1:n.*217-19C>A
ENST00000687740.1:n.3738-19C>A
ENST00000688151.1:n.2363-19C>A
ENST00000689271.1:c.900-19C>A ENSP00000510797.1:n.900-19C>A
ENST00000690900.1:c.*217-19C>A ENSP00000510703.1:n.*217-19C>A
ENST00000692212.1:n.2646C>A
ENST00000692355.1:c.306-19C>A
ENST00000692413.1:c.1035-19C>A ENSP00000509374.1:n.1035-19C>A
ENST00000692825.1:c.1121-19C>A ENSP00000509447.1:n.1121-19C>A
ENST00000693308.1:c.1101-19C>A ENSP00000509770.1:n.1101-19C>A
ENST00000693763.1:n.2213-19C>A
ENST00000245407.8:c.1053-19C>A MANE Select ENSP00000245407.3:n.1053-19C>A
ENST00000245407.7:c.1053-19C>A ENSP00000245407.3:n.1053-19C>A
ENST00000435065.6:c.1125-19C>A ENSP00000402760.2:n.1125-19C>A
ENST00000447841.5:c.111+1650C>A
ENST00000448810.5:c.401-105C>A
ENST00000461013.5:n.8475-19C>A
ENST00000475308.1:n.1712C>A
ENST00000479605.5:n.156-19C>A
NM_001308122.1:c.1125-19C>A NP_001295051.1:n.1125-19C>A
NM_003060.3:c.1053-19C>A NP_003051.1:n.1053-19C>A
XM_011543590.1:c.435-19C>A XP_011541892.1:n.435-19C>A
XR_427718.1:n.1413-19C>A
XR_948290.1:n.1393+1650C>A
XR_948291.1:n.1407-19C>A
XM_011543590.2:c.435-19C>A XP_011541892.1:n.435-19C>A
XM_017009778.2:c.525-19C>A XP_016865267.1:n.525-19C>A
XR_001742215.1:n.1394-105C>A
XR_001742216.1:n.1413-105C>A
XR_427718.2:n.1413-19C>A
XR_948290.2:n.1393+1650C>A
XR_948291.2:n.1407-19C>A
NM_003060.4:c.1053-19C>A MANE Select NP_003051.1:n.1053-19C>A
NM_001308122.2:c.1125-19C>A NP_001295051.1:n.1125-19C>A