Canonical Allele Identifier: CA2499223588

Gene: SLC12A3

Linked Data

• ClinVar Variation Id: 1172519
• ClinVar RCV Id: RCV001526394
• dbSNP Id: rs2144689577

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56870153del , CM000678.2:g.56870153del	GRCh38
NC_000016.9:g.56904065del , CM000678.1:g.56904065del	GRCh37
NC_000016.8:g.55461566del	NCBI36
NG_009386.1:g.9947del
NG_009386.2:g.9947del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563236.6:c.659del MANE Select	ENSP00000456149.2:p.Gly220AlafsTer?
ENST00000262502.5:c.656del	ENSP00000262502.5:p.Gly219AlafsTer?
ENST00000438926.6:c.659del	ENSP00000402152.2:p.Gly220AlafsTer?
ENST00000563236.5:c.659del	ENSP00000456149.1:p.Gly220AlafsTer?
ENST00000566786.5:c.656del	ENSP00000457552.1:p.Gly219AlafsTer?
NM_000339.2:c.659del	NP_000330.2:p.Gly220AlafsTer?
NM_001126107.1:c.656del	NP_001119579.1:p.Gly219AlafsTer?
NM_001126108.1:c.659del	NP_001119580.1:p.Gly220AlafsTer?
XM_005256119.1:c.656del	XP_005256176.1:p.Gly219AlafsTer?
XM_005256119.2:c.656del	XP_005256176.1:p.Gly219AlafsTer?
NM_000339.3:c.659del	NP_000330.3:p.Gly220AlafsTer?
NM_001126107.2:c.656del	NP_001119579.2:p.Gly219AlafsTer?
NM_001126108.2:c.659del MANE Select	NP_001119580.2:p.Gly220AlafsTer?