Canonical Allele Identifier: CA342760
Gene: SLC30A10 HGNC NCBI

Linked Data

ClinVar Variation Id: 30889
ClinVar RCV Id: RCV000023874
dbSNP Id: rs281860292

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.219915672del , CM000663.2:g.219915672del GRCh38
NC_000001.10:g.220089014del , CM000663.1:g.220089014del GRCh37
NC_000001.9:g.218155637del NCBI36
NG_032153.1:g.17980del
NG_032153.2:g.17980del

Transcript Alleles

HGVS Amino-acid Change
ENST00000696608.1:c.1046del ENSP00000512752.1:p.Gln349ArgfsTer26
ENST00000366926.4:c.1235del MANE Select ENSP00000355893.4:p.Gln412ArgfsTer26
ENST00000356609.2:c.*601del ENSP00000349018.2:n.*601del
ENST00000366926.3:c.1235del ENSP00000355893.3:p.Gln412ArgfsTer26
ENST00000484079.1:n.1053del
ENST00000484239.5:n.398+2583del
NM_018713.2:c.1235del NP_061183.2:p.Gln412ArgfsTer26
NR_046437.1:n.1484del
XM_006711437.2:c.1046del XP_006711500.2:p.Gln349ArgfsTer26
XM_011509727.1:c.560del XP_011508029.1:p.Gln187ArgfsTer26
XM_006711437.4:c.1046del XP_006711500.2:p.Gln349ArgfsTer26
XM_017001684.2:c.758del XP_016857173.1:p.Gln253ArgfsTer26
NM_001376929.1:c.1046del NP_001363858.1:p.Gln349ArgfsTer26
NM_018713.3:c.1235del MANE Select NP_061183.2:p.Gln412ArgfsTer26
NR_046437.2:n.1390del
NR_165031.1:n.1127del