Canonical Allele Identifier: CA380315241
Gene: SLC39A13 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47415154C>A , CM000673.2:g.47415154C>A GRCh38
NC_000011.9:g.47436705C>A , CM000673.1:g.47436705C>A GRCh37
NC_000011.8:g.47393281C>A NCBI36
NG_017073.1:g.11660C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000362021.9:c.1035C>A MANE Select ENSP00000354689.4:p.Asp345Glu
ENST00000354884.8:c.1014C>A ENSP00000346956.4:p.Asp338Glu
ENST00000362021.8:c.1035C>A ENSP00000354689.4:p.Asp345Glu
ENST00000524886.1:n.293C>A
ENST00000524928.1:c.*1237C>A ENSP00000437186.1:n.*1237C>A
ENST00000527829.1:n.267C>A
ENST00000533076.5:c.*32C>A ENSP00000434290.1:n.*32C>A
NM_001128225.2:c.1035C>A NP_001121697.1:p.Asp345Glu
NM_152264.4:c.1014C>A NP_689477.2:p.Asp338Glu
XM_006718381.2:c.1059C>A XP_006718444.1:p.Asp353Glu
XM_006718383.2:c.951C>A XP_006718446.1:p.Asp317Glu
XM_006718384.2:c.*32C>A XP_006718447.1:n.*32C>A
XM_006718385.2:c.*32C>A XP_006718448.1:n.*32C>A
XM_011520466.1:c.1080C>A XP_011518768.1:p.Asp360Glu
XM_011520467.1:c.1035C>A XP_011518769.1:p.Asp345Glu
XM_011520468.1:c.1035C>A XP_011518770.1:p.Asp345Glu
XM_011520469.1:c.972C>A XP_011518771.1:p.Asp324Glu
XM_011520470.1:c.927C>A XP_011518772.1:p.Asp309Glu
XR_242832.1:n.1420C>A
XR_428862.2:n.1095C>A
XR_428863.2:n.1091C>A
XR_930928.1:n.1116C>A
NM_001330245.1:c.*32C>A NP_001317174.1:n.*32C>A
NR_134854.1:n.1276C>A
XM_006718381.3:c.1059C>A XP_006718444.1:p.Asp353Glu
XM_006718383.3:c.951C>A XP_006718446.1:p.Asp317Glu
XM_011520468.3:c.1035C>A XP_011518770.1:p.Asp345Glu
XM_011520470.2:c.927C>A XP_011518772.1:p.Asp309Glu
XM_017018540.2:c.1014C>A XP_016874029.1:p.Asp338Glu
XM_017018541.2:c.906C>A XP_016874030.1:p.Asp302Glu
XM_024448762.1:c.1164C>A XP_024304530.1:p.Asp388Glu
XR_001748027.1:n.1235C>A
XR_001748028.1:n.1217C>A
XR_428862.3:n.1095C>A
XR_428863.3:n.1091C>A
XR_930928.2:n.1116C>A
NM_001128225.3:c.1035C>A MANE Select NP_001121697.2:p.Asp345Glu
NM_001330245.2:c.*32C>A NP_001317174.2:n.*32C>A
NM_152264.5:c.1014C>A NP_689477.3:p.Asp338Glu