Canonical Allele Identifier: CA5975676
Gene: SLC39A13 HGNC NCBI

Linked Data

ClinVar Variation Id: 2683148
ClinVar RCV Id: RCV003482015
dbSNP Id: rs766701277

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47410233C>G , CM000673.2:g.47410233C>G GRCh38
NC_000011.9:g.47431784C>G , CM000673.1:g.47431784C>G GRCh37
NC_000011.8:g.47388360C>G NCBI36
NG_017073.1:g.6739C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000362021.9:c.139C>G MANE Select ENSP00000354689.4:p.Arg47Gly
ENST00000354884.8:c.139C>G ENSP00000346956.4:p.Arg47Gly
ENST00000362021.8:c.139C>G ENSP00000354689.4:p.Arg47Gly
ENST00000524928.1:c.139C>G ENSP00000437186.1:p.Arg47Gly
ENST00000526614.5:c.139C>G ENSP00000432499.1:p.Arg47Gly
ENST00000527091.1:c.139C>G ENSP00000435076.1:p.Arg47Gly
ENST00000531419.5:c.139C>G ENSP00000432302.1:p.Arg47Gly
ENST00000531865.5:c.139C>G ENSP00000434684.1:p.Arg47Gly
ENST00000531974.5:c.139C>G ENSP00000435845.1:p.Arg47Gly
ENST00000533076.5:c.139C>G ENSP00000434290.1:p.Arg47Gly
NM_001128225.2:c.139C>G NP_001121697.1:p.Arg47Gly
NM_152264.4:c.139C>G NP_689477.2:p.Arg47Gly
XM_006718381.2:c.184C>G XP_006718444.1:p.Arg62Gly
XM_006718383.2:c.184C>G XP_006718446.1:p.Arg62Gly
XM_006718384.2:c.184C>G XP_006718447.1:p.Arg62Gly
XM_006718385.2:c.184C>G XP_006718448.1:p.Arg62Gly
XM_011520466.1:c.184C>G XP_011518768.1:p.Arg62Gly
XM_011520467.1:c.139C>G XP_011518769.1:p.Arg47Gly
XM_011520468.1:c.139C>G XP_011518770.1:p.Arg47Gly
XM_011520469.1:c.184C>G XP_011518771.1:p.Arg62Gly
XM_011520470.1:c.139C>G XP_011518772.1:p.Arg47Gly
XM_011520471.1:c.184C>G XP_011518773.1:p.Arg62Gly
XM_011520472.1:c.184C>G XP_011518774.1:p.Arg62Gly
XR_242832.1:n.549C>G
XR_428862.2:n.220C>G
XR_428863.2:n.220C>G
XR_930928.1:n.220C>G
NM_001330245.1:c.139C>G NP_001317174.1:p.Arg47Gly
NR_134854.1:n.405C>G
XM_006718381.3:c.184C>G XP_006718444.1:p.Arg62Gly
XM_006718383.3:c.184C>G XP_006718446.1:p.Arg62Gly
XM_011520468.3:c.139C>G XP_011518770.1:p.Arg47Gly
XM_011520470.2:c.139C>G XP_011518772.1:p.Arg47Gly
XM_017018540.2:c.139C>G XP_016874029.1:p.Arg47Gly
XM_017018541.2:c.139C>G XP_016874030.1:p.Arg47Gly
XM_024448762.1:c.139C>G XP_024304530.1:p.Arg47Gly
XR_001748027.1:n.220C>G
XR_001748028.1:n.220C>G
XR_428862.3:n.220C>G
XR_428863.3:n.220C>G
XR_930928.2:n.220C>G
NM_001128225.3:c.139C>G MANE Select NP_001121697.2:p.Arg47Gly
NM_001330245.2:c.139C>G NP_001317174.2:p.Arg47Gly
NM_152264.5:c.139C>G NP_689477.3:p.Arg47Gly