Canonical Allele Identifier: CA380315402
Gene: SLC39A13 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47415301C>G , CM000673.2:g.47415301C>G GRCh38
NC_000011.9:g.47436852C>G , CM000673.1:g.47436852C>G GRCh37
NC_000011.8:g.47393428C>G NCBI36
NG_017073.1:g.11807C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000362021.9:c.1054C>G MANE Select ENSP00000354689.4:p.Gln352Glu
ENST00000354884.8:c.1033C>G ENSP00000346956.4:p.Gln345Glu
ENST00000362021.8:c.1054C>G ENSP00000354689.4:p.Gln352Glu
ENST00000524886.1:n.312C>G
ENST00000524928.1:c.*1384C>G ENSP00000437186.1:n.*1384C>G
ENST00000527829.1:n.414C>G
ENST00000533076.5:c.*51C>G ENSP00000434290.1:n.*51C>G
NM_001128225.2:c.1054C>G NP_001121697.1:p.Gln352Glu
NM_152264.4:c.1033C>G NP_689477.2:p.Gln345Glu
XM_006718381.2:c.1078C>G XP_006718444.1:p.Gln360Glu
XM_006718383.2:c.970C>G XP_006718446.1:p.Gln324Glu
XM_006718384.2:c.*51C>G XP_006718447.1:n.*51C>G
XM_006718385.2:c.*51C>G XP_006718448.1:n.*51C>G
XM_011520466.1:c.1099C>G XP_011518768.1:p.Gln367Glu
XM_011520467.1:c.1054C>G XP_011518769.1:p.Gln352Glu
XM_011520468.1:c.1054C>G XP_011518770.1:p.Gln352Glu
XM_011520469.1:c.991C>G XP_011518771.1:p.Gln331Glu
XM_011520470.1:c.946C>G XP_011518772.1:p.Gln316Glu
XR_242832.1:n.1439C>G
XR_428862.2:n.1114C>G
XR_428863.2:n.1110C>G
XR_930928.1:n.1135C>G
NM_001330245.1:c.*51C>G NP_001317174.1:n.*51C>G
NR_134854.1:n.1295C>G
XM_006718381.3:c.1078C>G XP_006718444.1:p.Gln360Glu
XM_006718383.3:c.970C>G XP_006718446.1:p.Gln324Glu
XM_011520468.3:c.1054C>G XP_011518770.1:p.Gln352Glu
XM_011520470.2:c.946C>G XP_011518772.1:p.Gln316Glu
XM_017018540.2:c.1033C>G XP_016874029.1:p.Gln345Glu
XM_017018541.2:c.925C>G XP_016874030.1:p.Gln309Glu
XM_024448762.1:c.1183C>G XP_024304530.1:p.Gln395Glu
XR_001748027.1:n.1254C>G
XR_001748028.1:n.1236C>G
XR_428862.3:n.1114C>G
XR_428863.3:n.1110C>G
XR_930928.2:n.1135C>G
NM_001128225.3:c.1054C>G MANE Select NP_001121697.2:p.Gln352Glu
NM_001330245.2:c.*51C>G NP_001317174.2:n.*51C>G
NM_152264.5:c.1033C>G NP_689477.3:p.Gln345Glu