Canonical Allele Identifier: CA2689098970
Gene: SLC39A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.144414427_144414428del , CM000670.2:g.144414427_144414428del GRCh38
NC_000008.10:g.145639811_145639812del , CM000670.1:g.145639811_145639812del GRCh37
NC_000008.9:g.145610619_145610620del NCBI36
NG_012234.2:g.7464_7465del

Transcript Alleles

HGVS Amino-acid Change
ENST00000301305.8:c.984_985del MANE Select ENSP00000301305.4:p.Tyr329ArgfsTer?
ENST00000276833.9:c.909_910del ENSP00000276833.5:p.Tyr304ArgfsTer?
ENST00000301305.7:c.984_985del ENSP00000301305.3:p.Tyr329ArgfsTer?
NM_017767.2:c.909_910del NP_060237.2:p.Tyr304ArgfsTer?
NM_130849.3:c.984_985del NP_570901.2:p.Tyr329ArgfsTer?
XM_006716599.1:c.984_985del XP_006716662.1:p.Tyr329ArgfsTer?
XM_011517153.1:c.702_703del XP_011515455.1:p.Tyr235ArgfsTer?
XM_024447188.1:c.702_703del XP_024302956.1:p.Tyr235ArgfsTer?
XM_024447189.1:c.702_703del XP_024302957.1:p.Tyr235ArgfsTer?
NM_001374839.1:c.702_703del NP_001361768.1:p.Tyr235ArgfsTer?
NM_017767.3:c.909_910del NP_060237.3:p.Tyr304ArgfsTer?
NM_130849.4:c.984_985del MANE Select NP_570901.3:p.Tyr329ArgfsTer?