Canonical Allele Identifier: CA2576001904
Gene: SLC12A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56870035del , CM000678.2:g.56870035del GRCh38
NC_000016.9:g.56903947del , CM000678.1:g.56903947del GRCh37
NC_000016.8:g.55461448del NCBI36
NG_009386.1:g.9829del
NG_009386.2:g.9829del

Transcript Alleles

HGVS Amino-acid change
ENST00000563236.6:c.602-61del MANE Select ENSP00000456149.2:n.602-61del
ENST00000262502.5:c.599-61del ENSP00000262502.5:n.599-61del
ENST00000438926.6:c.602-61del ENSP00000402152.2:n.602-61del
ENST00000563236.5:c.602-61del ENSP00000456149.1:n.602-61del
ENST00000566786.5:c.599-61del ENSP00000457552.1:n.599-61del
NM_000339.2:c.602-61del NP_000330.2:n.602-61del
NM_001126107.1:c.599-61del NP_001119579.1:n.599-61del
NM_001126108.1:c.602-61del NP_001119580.1:n.602-61del
XM_005256119.1:c.599-61del XP_005256176.1:n.599-61del
XM_005256119.2:c.599-61del XP_005256176.1:n.599-61del
NM_000339.3:c.602-61del NP_000330.3:n.602-61del
NM_001126107.2:c.599-61del NP_001119579.2:n.599-61del
NM_001126108.2:c.602-61del MANE Select NP_001119580.2:n.602-61del