Canonical Allele Identifier: CA8069577
Gene: SLC12A3 HGNC NCBI

Linked Data

dbSNP Id: rs778213007

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56884077_56884079del , CM000678.2:g.56884077_56884079del GRCh38
NC_000016.9:g.56917989_56917991del , CM000678.1:g.56917989_56917991del GRCh37
NC_000016.8:g.55475490_55475492del NCBI36
NG_009386.1:g.23871_23873del
NG_009386.2:g.23871_23873del

Transcript Alleles

HGVS Amino-acid Change
ENST00000563236.6:c.1698_1700del MANE Select ENSP00000456149.2:p.Asn566del
ENST00000262502.5:c.1695_1697del ENSP00000262502.5:p.Asn565del
ENST00000438926.6:c.1698_1700del ENSP00000402152.2:p.Asn566del
ENST00000563236.5:c.1698_1700del ENSP00000456149.1:p.Asn566del
ENST00000566786.5:c.1695_1697del ENSP00000457552.1:p.Asn565del
NM_000339.2:c.1698_1700del NP_000330.2:p.Asn566del
NM_001126107.1:c.1695_1697del NP_001119579.1:p.Asn565del
NM_001126108.1:c.1698_1700del NP_001119580.1:p.Asn566del
XM_005256119.1:c.1695_1697del XP_005256176.1:p.Asn565del
XM_005256119.2:c.1695_1697del XP_005256176.1:p.Asn565del
NM_000339.3:c.1698_1700del NP_000330.3:p.Asn566del
NM_001126107.2:c.1695_1697del NP_001119579.2:p.Asn565del
NM_001126108.2:c.1698_1700del MANE Select NP_001119580.2:p.Asn566del