Canonical Allele Identifier: CA380315233
Gene: SLC39A13 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47415152G>C , CM000673.2:g.47415152G>C GRCh38
NC_000011.9:g.47436703G>C , CM000673.1:g.47436703G>C GRCh37
NC_000011.8:g.47393279G>C NCBI36
NG_017073.1:g.11658G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000362021.9:c.1033G>C MANE Select ENSP00000354689.4:p.Asp345His
ENST00000354884.8:c.1012G>C ENSP00000346956.4:p.Asp338His
ENST00000362021.8:c.1033G>C ENSP00000354689.4:p.Asp345His
ENST00000524886.1:n.291G>C
ENST00000524928.1:c.*1235G>C ENSP00000437186.1:n.*1235G>C
ENST00000527829.1:n.265G>C
ENST00000533076.5:c.*30G>C ENSP00000434290.1:n.*30G>C
NM_001128225.2:c.1033G>C NP_001121697.1:p.Asp345His
NM_152264.4:c.1012G>C NP_689477.2:p.Asp338His
XM_006718381.2:c.1057G>C XP_006718444.1:p.Asp353His
XM_006718383.2:c.949G>C XP_006718446.1:p.Asp317His
XM_006718384.2:c.*30G>C XP_006718447.1:n.*30G>C
XM_006718385.2:c.*30G>C XP_006718448.1:n.*30G>C
XM_011520466.1:c.1078G>C XP_011518768.1:p.Asp360His
XM_011520467.1:c.1033G>C XP_011518769.1:p.Asp345His
XM_011520468.1:c.1033G>C XP_011518770.1:p.Asp345His
XM_011520469.1:c.970G>C XP_011518771.1:p.Asp324His
XM_011520470.1:c.925G>C XP_011518772.1:p.Asp309His
XR_242832.1:n.1418G>C
XR_428862.2:n.1093G>C
XR_428863.2:n.1089G>C
XR_930928.1:n.1114G>C
NM_001330245.1:c.*30G>C NP_001317174.1:n.*30G>C
NR_134854.1:n.1274G>C
XM_006718381.3:c.1057G>C XP_006718444.1:p.Asp353His
XM_006718383.3:c.949G>C XP_006718446.1:p.Asp317His
XM_011520468.3:c.1033G>C XP_011518770.1:p.Asp345His
XM_011520470.2:c.925G>C XP_011518772.1:p.Asp309His
XM_017018540.2:c.1012G>C XP_016874029.1:p.Asp338His
XM_017018541.2:c.904G>C XP_016874030.1:p.Asp302His
XM_024448762.1:c.1162G>C XP_024304530.1:p.Asp388His
XR_001748027.1:n.1233G>C
XR_001748028.1:n.1215G>C
XR_428862.3:n.1093G>C
XR_428863.3:n.1089G>C
XR_930928.2:n.1114G>C
NM_001128225.3:c.1033G>C MANE Select NP_001121697.2:p.Asp345His
NM_001330245.2:c.*30G>C NP_001317174.2:n.*30G>C
NM_152264.5:c.1012G>C NP_689477.3:p.Asp338His