Canonical Allele Identifier: CA2838361224
Gene: SLC12A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56870780del , CM000678.2:g.56870780del GRCh38
NC_000016.9:g.56904692del , CM000678.1:g.56904692del GRCh37
NC_000016.8:g.55462193del NCBI36
NG_009386.1:g.10574del
NG_009386.2:g.10574del

Transcript Alleles

HGVS Amino-acid Change
ENST00000563236.6:c.852+44del MANE Select ENSP00000456149.2:n.852+44del
ENST00000262502.5:c.849+44del ENSP00000262502.5:n.849+44del
ENST00000438926.6:c.852+44del ENSP00000402152.2:n.852+44del
ENST00000563236.5:c.852+44del ENSP00000456149.1:n.852+44del
ENST00000566786.5:c.849+44del ENSP00000457552.1:n.849+44del
NM_000339.2:c.852+44del NP_000330.2:n.852+44del
NM_001126107.1:c.849+44del NP_001119579.1:n.849+44del
NM_001126108.1:c.852+44del NP_001119580.1:n.852+44del
XM_005256119.1:c.849+44del XP_005256176.1:n.849+44del
XM_005256119.2:c.849+44del XP_005256176.1:n.849+44del
NM_000339.3:c.852+44del NP_000330.3:n.852+44del
NM_001126107.2:c.849+44del NP_001119579.2:n.849+44del
NM_001126108.2:c.852+44del MANE Select NP_001119580.2:n.852+44del