Canonical Allele Identifier: CA658657748

Gene: SLC39A14

Linked Data

• ClinVar Variation Id: 446707
• ClinVar RCV Id: RCV000515834
• dbSNP Id: rs1039778197
• MyVariant Identifiers: chr8:g.22273273C>G (hg19) ; chr8:g.22415760C>G (hg38)
• PubMed: PMID:28541650

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.22415760C>G , CM000670.2:g.22415760C>G	GRCh38
NC_000008.10:g.22273273C>G , CM000670.1:g.22273273C>G	GRCh37
NC_000008.9:g.22329218C>G	NCBI36
NG_054890.1:g.53512C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000359741.10:c.751-9C>G MANE Plus Clinical	ENSP00000352779.5:n.751-9C>G
ENST00000381237.6:c.751-9C>G MANE Select	ENSP00000370635.1:n.751-9C>G
ENST00000240095.10:c.751-9C>G	ENSP00000240095.6:n.751-9C>G
ENST00000289952.9:c.751-9C>G	ENSP00000289952.5:n.751-9C>G
ENST00000359741.9:c.751-9C>G	ENSP00000352779.5:n.751-9C>G
ENST00000381237.5:c.751-9C>G	ENSP00000370635.1:n.751-9C>G
ENST00000517370.1:c.220-9C>G	ENSP00000427981.1:n.220-9C>G
ENST00000518348.1:n.634C>G
NM_001128431.2:c.751-9C>G	NP_001121903.1:n.751-9C>G
NM_001135153.1:c.751-9C>G	NP_001128625.1:n.751-9C>G
NM_001135154.1:c.751-9C>G	NP_001128626.1:n.751-9C>G
NM_015359.4:c.751-9C>G	NP_056174.2:n.751-9C>G
XM_005273463.1:c.781-9C>G	XP_005273520.1:n.781-9C>G
XM_005273465.1:c.751-9C>G	XP_005273522.1:n.751-9C>G
XM_005273466.3:c.751-9C>G	XP_005273523.1:n.751-9C>G
XM_006716323.1:c.781-9C>G	XP_006716386.1:n.781-9C>G
XM_006716324.1:c.751-9C>G	XP_006716387.1:n.751-9C>G
XM_011544477.1:c.751-9C>G	XP_011542779.1:n.751-9C>G
XM_011544478.1:c.751-9C>G	XP_011542780.1:n.751-9C>G
NM_001128431.3:c.751-9C>G	NP_001121903.1:n.751-9C>G
NM_001135153.2:c.751-9C>G	NP_001128625.1:n.751-9C>G
NM_001135154.2:c.751-9C>G	NP_001128626.1:n.751-9C>G
NM_001351655.1:c.751-9C>G	NP_001338584.1:n.751-9C>G
NM_001351656.1:c.751-9C>G	NP_001338585.1:n.751-9C>G
NM_001351657.1:c.781-9C>G	NP_001338586.1:n.781-9C>G
NM_001351658.1:c.781-9C>G	NP_001338587.1:n.781-9C>G
NM_001351659.1:c.781-9C>G	NP_001338588.1:n.781-9C>G
NM_001351660.1:c.751-9C>G	NP_001338589.1:n.751-9C>G
NM_015359.5:c.751-9C>G	NP_056174.2:n.751-9C>G
XM_005273466.4:c.751-9C>G	XP_005273523.1:n.751-9C>G
XM_006716324.3:c.751-9C>G	XP_006716387.1:n.751-9C>G
XM_011544478.3:c.751-9C>G	XP_011542780.1:n.751-9C>G
XM_017013293.2:c.781-9C>G	XP_016868782.1:n.781-9C>G
NM_001128431.4:c.751-9C>G MANE Select	NP_001121903.1:n.751-9C>G
NM_001135153.3:c.751-9C>G	NP_001128625.1:n.751-9C>G
NM_001135154.3:c.751-9C>G	NP_001128626.1:n.751-9C>G
NM_001351655.2:c.751-9C>G	NP_001338584.1:n.751-9C>G
NM_001351656.2:c.751-9C>G	NP_001338585.1:n.751-9C>G
NM_001351657.2:c.781-9C>G	NP_001338586.1:n.781-9C>G
NM_001351658.2:c.781-9C>G	NP_001338587.1:n.781-9C>G
NM_001351659.2:c.781-9C>G	NP_001338588.1:n.781-9C>G
NM_001351660.2:c.751-9C>G	NP_001338589.1:n.751-9C>G
NM_015359.6:c.751-9C>G MANE Plus Clinical	NP_056174.2:n.751-9C>G