Canonical Allele Identifier: CA3403778
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 379259
dbSNP Id: rs772578415

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132370049G>A , CM000667.2:g.132370049G>A GRCh38
NC_000005.9:g.131705741G>A , CM000667.1:g.131705741G>A GRCh37
NC_000005.8:g.131733640G>A NCBI36
NG_008982.1:g.5341G>A
NG_008982.2:g.5346G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000415928.6:c.77G>A ENSP00000388838.2:p.Ser26Asn
ENST00000435065.7:c.77G>A ENSP00000402760.2:p.Ser26Asn
ENST00000448810.6:c.77G>A ENSP00000401860.2:p.Ser26Asn
ENST00000686757.1:c.77G>A ENSP00000510721.1:p.Ser26Asn
ENST00000687740.1:n.211G>A
ENST00000689271.1:c.77G>A ENSP00000510797.1:p.Ser26Asn
ENST00000690900.1:c.77G>A ENSP00000510703.1:p.Ser26Asn
ENST00000692413.1:c.77G>A ENSP00000509374.1:p.Ser26Asn
ENST00000692825.1:c.77G>A ENSP00000509447.1:p.Ser26Asn
ENST00000693308.1:c.77G>A ENSP00000509770.1:p.Ser26Asn
ENST00000693763.1:n.211G>A
ENST00000245407.8:c.77G>A MANE Select ENSP00000245407.3:p.Ser26Asn
ENST00000245407.7:c.77G>A ENSP00000245407.3:p.Ser26Asn
ENST00000435065.6:c.77G>A ENSP00000402760.2:p.Ser26Asn
ENST00000437841.6:c.77G>A ENSP00000400553.1:p.Ser26Asn
NM_001308122.1:c.77G>A NP_001295051.1:p.Ser26Asn
NM_003060.3:c.77G>A NP_003051.1:p.Ser26Asn
XR_427718.1:n.346G>A
XR_948290.1:n.346G>A
XR_948291.1:n.346G>A
XR_001742215.1:n.346G>A
XR_001742216.1:n.346G>A
XR_427718.2:n.346G>A
XR_948290.2:n.346G>A
XR_948291.2:n.346G>A
NM_003060.4:c.77G>A MANE Select NP_003051.1:p.Ser26Asn
NM_001308122.2:c.77G>A NP_001295051.1:p.Ser26Asn