Canonical Allele Identifier: CA1826307134
Gene: SLC39A4 HGNC NCBI

Linked Data

dbSNP Id: rs1822073924

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.144414392_144414400dup , CM000670.2:g.144414392_144414400dup GRCh38
NC_000008.10:g.145639776_145639784dup , CM000670.1:g.145639776_145639784dup GRCh37
NC_000008.9:g.145610584_145610592dup NCBI36
NG_012234.2:g.7492_7500dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000301305.8:c.1012_1020dup MANE Select ENSP00000301305.4:p.Cys340_Ala341insCysLeuCys
ENST00000276833.9:c.937_945dup ENSP00000276833.5:p.Cys315_Ala316insCysLeuCys
ENST00000301305.7:c.1012_1020dup ENSP00000301305.3:p.Cys340_Ala341insCysLeuCys
NM_017767.2:c.937_945dup NP_060237.2:p.Cys315_Ala316insCysLeuCys
NM_130849.3:c.1012_1020dup NP_570901.2:p.Cys340_Ala341insCysLeuCys
XM_006716599.1:c.1012_1020dup XP_006716662.1:p.Cys340_Ala341insCysLeuCys
XM_011517153.1:c.730_738dup XP_011515455.1:p.Cys246_Ala247insCysLeuCys
XM_024447188.1:c.730_738dup XP_024302956.1:p.Cys246_Ala247insCysLeuCys
XM_024447189.1:c.730_738dup XP_024302957.1:p.Cys246_Ala247insCysLeuCys
NM_001374839.1:c.730_738dup NP_001361768.1:p.Cys246_Ala247insCysLeuCys
NM_017767.3:c.937_945dup NP_060237.3:p.Cys315_Ala316insCysLeuCys
NM_130849.4:c.1012_1020dup MANE Select NP_570901.3:p.Cys340_Ala341insCysLeuCys