Canonical Allele Identifier: CA372621212
Gene: SLC39A4 HGNC NCBI

Linked Data

dbSNP Id: rs1586651882

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.144414333T>C , CM000670.2:g.144414333T>C GRCh38
NC_000008.10:g.145639717T>C , CM000670.1:g.145639717T>C GRCh37
NC_000008.9:g.145610525T>C NCBI36
NG_012234.2:g.7558A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000301305.8:c.1078A>G MANE Select ENSP00000301305.4:p.Ile360Val
ENST00000276833.9:c.1003A>G ENSP00000276833.5:p.Ile335Val
ENST00000301305.7:c.1078A>G ENSP00000301305.3:p.Ile360Val
NM_017767.2:c.1003A>G NP_060237.2:p.Ile335Val
NM_130849.3:c.1078A>G NP_570901.2:p.Ile360Val
XM_006716599.1:c.1078A>G XP_006716662.1:p.Ile360Val
XM_011517153.1:c.796A>G XP_011515455.1:p.Ile266Val
XM_024447188.1:c.796A>G XP_024302956.1:p.Ile266Val
XM_024447189.1:c.796A>G XP_024302957.1:p.Ile266Val
NM_001374839.1:c.796A>G NP_001361768.1:p.Ile266Val
NM_017767.3:c.1003A>G NP_060237.3:p.Ile335Val
NM_130849.4:c.1078A>G MANE Select NP_570901.3:p.Ile360Val