Canonical Allele Identifier: CA10584027
Gene: SLC39A14 HGNC NCBI

Linked Data

ClinVar Variation Id: 242924
ClinVar RCV Id: RCV000234926
dbSNP Id: rs879253763
MyVariant Identifiers: chr8:g.22265844T>G (hg19) chr8:g.22408331T>G (hg38)
PubMed: PMID:27231142 PMID:28541650
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.22408331T>G , CM000670.2:g.22408331T>G GRCh38
NC_000008.10:g.22265844T>G , CM000670.1:g.22265844T>G GRCh37
NC_000008.9:g.22321789T>G NCBI36
NG_054890.1:g.46083T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000359741.10:c.292T>G MANE Plus Clinical ENSP00000352779.5:p.Phe98Val
ENST00000381237.6:c.292T>G MANE Select ENSP00000370635.1:p.Phe98Val
ENST00000240095.10:c.292T>G ENSP00000240095.6:p.Phe98Val
ENST00000289952.9:c.292T>G ENSP00000289952.5:p.Phe98Val
ENST00000359741.9:c.292T>G ENSP00000352779.5:p.Phe98Val
ENST00000381237.5:c.292T>G ENSP00000370635.1:p.Phe98Val
ENST00000517552.1:c.292T>G ENSP00000430564.1:p.Phe98Val
ENST00000519960.5:c.292T>G ENSP00000430629.1:p.Phe98Val
ENST00000522881.2:c.292T>G ENSP00000429328.2:p.Phe98Val
NM_001128431.2:c.292T>G NP_001121903.1:p.Phe98Val
NM_001135153.1:c.292T>G NP_001128625.1:p.Phe98Val
NM_001135154.1:c.292T>G NP_001128626.1:p.Phe98Val
NM_015359.4:c.292T>G NP_056174.2:p.Phe98Val
XM_005273463.1:c.322T>G XP_005273520.1:p.Phe108Val
XM_005273465.1:c.292T>G XP_005273522.1:p.Phe98Val
XM_005273466.3:c.292T>G XP_005273523.1:p.Phe98Val
XM_006716323.1:c.322T>G XP_006716386.1:p.Phe108Val
XM_006716324.1:c.292T>G XP_006716387.1:p.Phe98Val
XM_011544477.1:c.292T>G XP_011542779.1:p.Phe98Val
XM_011544478.1:c.292T>G XP_011542780.1:p.Phe98Val
NM_001128431.3:c.292T>G NP_001121903.1:p.Phe98Val
NM_001135153.2:c.292T>G NP_001128625.1:p.Phe98Val
NM_001135154.2:c.292T>G NP_001128626.1:p.Phe98Val
NM_001351655.1:c.292T>G NP_001338584.1:p.Phe98Val
NM_001351656.1:c.292T>G NP_001338585.1:p.Phe98Val
NM_001351657.1:c.322T>G NP_001338586.1:p.Phe108Val
NM_001351658.1:c.322T>G NP_001338587.1:p.Phe108Val
NM_001351659.1:c.322T>G NP_001338588.1:p.Phe108Val
NM_001351660.1:c.292T>G NP_001338589.1:p.Phe98Val
NM_015359.5:c.292T>G NP_056174.2:p.Phe98Val
XM_005273466.4:c.292T>G XP_005273523.1:p.Phe98Val
XM_006716324.3:c.292T>G XP_006716387.1:p.Phe98Val
XM_011544478.3:c.292T>G XP_011542780.1:p.Phe98Val
XM_017013293.2:c.322T>G XP_016868782.1:p.Phe108Val
NM_001128431.4:c.292T>G MANE Select NP_001121903.1:p.Phe98Val
NM_001135153.3:c.292T>G NP_001128625.1:p.Phe98Val
NM_001135154.3:c.292T>G NP_001128626.1:p.Phe98Val
NM_001351655.2:c.292T>G NP_001338584.1:p.Phe98Val
NM_001351656.2:c.292T>G NP_001338585.1:p.Phe98Val
NM_001351657.2:c.322T>G NP_001338586.1:p.Phe108Val
NM_001351658.2:c.322T>G NP_001338587.1:p.Phe108Val
NM_001351659.2:c.322T>G NP_001338588.1:p.Phe108Val
NM_001351660.2:c.292T>G NP_001338589.1:p.Phe98Val
NM_015359.6:c.292T>G MANE Plus Clinical NP_056174.2:p.Phe98Val
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