Canonical Allele Identifier: CA2613414204
Gene: SLC39A13 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47415160del , CM000673.2:g.47415160del GRCh38
NC_000011.9:g.47436711del , CM000673.1:g.47436711del GRCh37
NC_000011.8:g.47393287del NCBI36
NG_017073.1:g.11666del

Transcript Alleles

HGVS Amino-acid Change
ENST00000362021.9:c.1040+1del
ENST00000354884.8:c.1019+1del
ENST00000362021.8:c.1040+1del
ENST00000524886.1:n.298+1del
ENST00000524928.1:c.*1243del ENSP00000437186.1:n.*1243del
ENST00000527829.1:n.273del
ENST00000533076.5:c.*37+1del
NM_001128225.2:c.1040+1del
NM_152264.4:c.1019+1del
XM_006718381.2:c.1064+1del
XM_006718383.2:c.956+1del
XM_006718384.2:c.*37+1del
XM_006718385.2:c.*37+1del
XM_011520466.1:c.1085+1del
XM_011520467.1:c.1040+1del
XM_011520468.1:c.1040+1del
XM_011520469.1:c.977+1del
XM_011520470.1:c.932+1del
XR_242832.1:n.1425+1del
XR_428862.2:n.1100+1del
XR_428863.2:n.1096+1del
XR_930928.1:n.1121+1del
NM_001330245.1:c.*37+1del
NR_134854.1:n.1281+1del
XM_006718381.3:c.1064+1del
XM_006718383.3:c.956+1del
XM_011520468.3:c.1040+1del
XM_011520470.2:c.932+1del
XM_017018540.2:c.1019+1del
XM_017018541.2:c.911+1del
XM_024448762.1:c.1169+1del
XR_001748027.1:n.1240+1del
XR_001748028.1:n.1222+1del
XR_428862.3:n.1100+1del
XR_428863.3:n.1096+1del
XR_930928.2:n.1121+1del
NM_001128225.3:c.1040+1del
NM_001330245.2:c.*37+1del
NM_152264.5:c.1019+1del