Canonical Allele Identifier: CA2689098813
Gene: SLC39A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.144414356_144414378del , CM000670.2:g.144414356_144414378del GRCh38
NC_000008.10:g.145639740_145639762del , CM000670.1:g.145639740_145639762del GRCh37
NC_000008.9:g.145610548_145610570del NCBI36
NG_012234.2:g.7515_7537del

Transcript Alleles

HGVS Amino-acid Change
ENST00000301305.8:c.1035_1057del MANE Select ENSP00000301305.4:p.Leu346GlnfsTer?
ENST00000276833.9:c.960_982del ENSP00000276833.5:p.Leu321GlnfsTer?
ENST00000301305.7:c.1035_1057del ENSP00000301305.3:p.Leu346GlnfsTer?
NM_017767.2:c.960_982del NP_060237.2:p.Leu321GlnfsTer?
NM_130849.3:c.1035_1057del NP_570901.2:p.Leu346GlnfsTer?
XM_006716599.1:c.1035_1057del XP_006716662.1:p.Leu346GlnfsTer?
XM_011517153.1:c.753_775del XP_011515455.1:p.Leu252GlnfsTer?
XM_024447188.1:c.753_775del XP_024302956.1:p.Leu252GlnfsTer?
XM_024447189.1:c.753_775del XP_024302957.1:p.Leu252GlnfsTer?
NM_001374839.1:c.753_775del NP_001361768.1:p.Leu252GlnfsTer?
NM_017767.3:c.960_982del NP_060237.3:p.Leu321GlnfsTer?
NM_130849.4:c.1035_1057del MANE Select NP_570901.3:p.Leu346GlnfsTer?