Canonical Allele Identifier: CA380315476
Gene: SLC39A13 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47415318T>G , CM000673.2:g.47415318T>G GRCh38
NC_000011.9:g.47436869T>G , CM000673.1:g.47436869T>G GRCh37
NC_000011.8:g.47393445T>G NCBI36
NG_017073.1:g.11824T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000362021.9:c.1071T>G MANE Select ENSP00000354689.4:p.Cys357Trp
ENST00000354884.8:c.1050T>G ENSP00000346956.4:p.Cys350Trp
ENST00000362021.8:c.1071T>G ENSP00000354689.4:p.Cys357Trp
ENST00000524886.1:n.329T>G
ENST00000524928.1:c.*1401T>G ENSP00000437186.1:n.*1401T>G
ENST00000527829.1:n.431T>G
ENST00000533076.5:c.*68T>G ENSP00000434290.1:n.*68T>G
NM_001128225.2:c.1071T>G NP_001121697.1:p.Cys357Trp
NM_152264.4:c.1050T>G NP_689477.2:p.Cys350Trp
XM_006718381.2:c.1095T>G XP_006718444.1:p.Cys365Trp
XM_006718383.2:c.987T>G XP_006718446.1:p.Cys329Trp
XM_006718384.2:c.*68T>G XP_006718447.1:n.*68T>G
XM_006718385.2:c.*68T>G XP_006718448.1:n.*68T>G
XM_011520466.1:c.1116T>G XP_011518768.1:p.Cys372Trp
XM_011520467.1:c.1071T>G XP_011518769.1:p.Cys357Trp
XM_011520468.1:c.1071T>G XP_011518770.1:p.Cys357Trp
XM_011520469.1:c.1008T>G XP_011518771.1:p.Cys336Trp
XM_011520470.1:c.963T>G XP_011518772.1:p.Cys321Trp
XR_242832.1:n.1456T>G
XR_428862.2:n.1131T>G
XR_428863.2:n.1127T>G
XR_930928.1:n.1152T>G
NM_001330245.1:c.*68T>G NP_001317174.1:n.*68T>G
NR_134854.1:n.1312T>G
XM_006718381.3:c.1095T>G XP_006718444.1:p.Cys365Trp
XM_006718383.3:c.987T>G XP_006718446.1:p.Cys329Trp
XM_011520468.3:c.1071T>G XP_011518770.1:p.Cys357Trp
XM_011520470.2:c.963T>G XP_011518772.1:p.Cys321Trp
XM_017018540.2:c.1050T>G XP_016874029.1:p.Cys350Trp
XM_017018541.2:c.942T>G XP_016874030.1:p.Cys314Trp
XM_024448762.1:c.1200T>G XP_024304530.1:p.Cys400Trp
XR_001748027.1:n.1271T>G
XR_001748028.1:n.1253T>G
XR_428862.3:n.1131T>G
XR_428863.3:n.1127T>G
XR_930928.2:n.1152T>G
NM_001128225.3:c.1071T>G MANE Select NP_001121697.2:p.Cys357Trp
NM_001330245.2:c.*68T>G NP_001317174.2:n.*68T>G
NM_152264.5:c.1050T>G NP_689477.3:p.Cys350Trp