Canonical Allele Identifier: CA342607
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 25350
dbSNP Id: rs11568520

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132370023C>G , CM000667.2:g.132370023C>G GRCh38
NC_000005.9:g.131705715C>G , CM000667.1:g.131705715C>G GRCh37
NC_000005.8:g.131733614C>G NCBI36
NG_008982.1:g.5315C>G
NG_008982.2:g.5320C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000415928.6:c.51C>G ENSP00000388838.2:p.Phe17Leu
ENST00000435065.7:c.51C>G ENSP00000402760.2:p.Phe17Leu
ENST00000448810.6:c.51C>G ENSP00000401860.2:p.Phe17Leu
ENST00000686757.1:c.51C>G ENSP00000510721.1:p.Phe17Leu
ENST00000687740.1:n.185C>G
ENST00000689271.1:c.51C>G ENSP00000510797.1:p.Phe17Leu
ENST00000690900.1:c.51C>G ENSP00000510703.1:p.Phe17Leu
ENST00000692413.1:c.51C>G ENSP00000509374.1:p.Phe17Leu
ENST00000692825.1:c.51C>G ENSP00000509447.1:p.Phe17Leu
ENST00000693308.1:c.51C>G ENSP00000509770.1:p.Phe17Leu
ENST00000693763.1:n.185C>G
ENST00000245407.8:c.51C>G MANE Select ENSP00000245407.3:p.Phe17Leu
ENST00000245407.7:c.51C>G ENSP00000245407.3:p.Phe17Leu
ENST00000435065.6:c.51C>G ENSP00000402760.2:p.Phe17Leu
ENST00000437841.6:c.51C>G ENSP00000400553.1:p.Phe17Leu
NM_001308122.1:c.51C>G NP_001295051.1:p.Phe17Leu
NM_003060.3:c.51C>G NP_003051.1:p.Phe17Leu
XR_427718.1:n.320C>G
XR_948290.1:n.320C>G
XR_948291.1:n.320C>G
XR_001742215.1:n.320C>G
XR_001742216.1:n.320C>G
XR_427718.2:n.320C>G
XR_948290.2:n.320C>G
XR_948291.2:n.320C>G
NM_003060.4:c.51C>G MANE Select NP_003051.1:p.Phe17Leu
NM_001308122.2:c.51C>G NP_001295051.1:p.Phe17Leu