Canonical Allele Identifier: CA2689098887
Gene: SLC39A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.144414364_144414370dup , CM000670.2:g.144414364_144414370dup GRCh38
NC_000008.10:g.145639748_145639754dup , CM000670.1:g.145639748_145639754dup GRCh37
NC_000008.9:g.145610556_145610562dup NCBI36
NG_012234.2:g.7521_7527dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000301305.8:c.1041_1047dup MANE Select ENSP00000301305.4:p.Cys350AlafsTer?
ENST00000276833.9:c.966_972dup ENSP00000276833.5:p.Cys325AlafsTer?
ENST00000301305.7:c.1041_1047dup ENSP00000301305.3:p.Cys350AlafsTer?
NM_017767.2:c.966_972dup NP_060237.2:p.Cys325AlafsTer?
NM_130849.3:c.1041_1047dup NP_570901.2:p.Cys350AlafsTer?
XM_006716599.1:c.1041_1047dup XP_006716662.1:p.Cys350AlafsTer?
XM_011517153.1:c.759_765dup XP_011515455.1:p.Cys256AlafsTer?
XM_024447188.1:c.759_765dup XP_024302956.1:p.Cys256AlafsTer?
XM_024447189.1:c.759_765dup XP_024302957.1:p.Cys256AlafsTer?
NM_001374839.1:c.759_765dup NP_001361768.1:p.Cys256AlafsTer?
NM_017767.3:c.966_972dup NP_060237.3:p.Cys325AlafsTer?
NM_130849.4:c.1041_1047dup MANE Select NP_570901.3:p.Cys350AlafsTer?