Canonical Allele Identifier: CA3403778

Gene: SLC22A5

Linked Data

• ClinVar Variation Id: 379259
• ClinVar RCV Id: RCV000439652 ; RCV001237032
• dbSNP Id: rs772578415
• ExAC: 5:131705741 G / A
• gnomAD v2: 5-131705741-G-A
• gnomAD v3: 5-132370049-G-A
• gnomAD v4: 5-132370049-G-A
• MyVariant Identifiers: chr5:g.131705741G>A (hg19) ; chr5:g.132370049G>A (hg38)

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