Canonical Allele Identifier: CA1969373849
Gene: SLC39A13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47415309T= , CM000673.2:g.47415309T= GRCh38
NC_000011.9:g.47436860T= , CM000673.1:g.47436860T= GRCh37
NC_000011.8:g.47393436T= NCBI36
NG_017073.1:g.11815T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000362021.9:c.1062T= MANE Select ENSP00000354689.4:p.Leu354=
ENST00000354884.8:c.1041T= ENSP00000346956.4:p.Leu347=
ENST00000362021.8:c.1062T= ENSP00000354689.4:p.Leu354=
ENST00000524886.1:n.320T=
ENST00000524928.1:c.*1392T= ENSP00000437186.1:n.*1392T=
ENST00000527829.1:n.422T=
ENST00000533076.5:c.*59T= ENSP00000434290.1:n.*59T=
NM_001128225.2:c.1062T= NP_001121697.1:p.Leu354=
NM_152264.4:c.1041T= NP_689477.2:p.Leu347=
XM_006718381.2:c.1086T= XP_006718444.1:p.Leu362=
XM_006718383.2:c.978T= XP_006718446.1:p.Leu326=
XM_006718384.2:c.*59T= XP_006718447.1:n.*59T=
XM_006718385.2:c.*59T= XP_006718448.1:n.*59T=
XM_011520466.1:c.1107T= XP_011518768.1:p.Leu369=
XM_011520467.1:c.1062T= XP_011518769.1:p.Leu354=
XM_011520468.1:c.1062T= XP_011518770.1:p.Leu354=
XM_011520469.1:c.999T= XP_011518771.1:p.Leu333=
XM_011520470.1:c.954T= XP_011518772.1:p.Leu318=
XR_242832.1:n.1447T=
XR_428862.2:n.1122T=
XR_428863.2:n.1118T=
XR_930928.1:n.1143T=
NM_001330245.1:c.*59T= NP_001317174.1:n.*59T=
NR_134854.1:n.1303T=
XM_006718381.3:c.1086T= XP_006718444.1:p.Leu362=
XM_006718383.3:c.978T= XP_006718446.1:p.Leu326=
XM_011520468.3:c.1062T= XP_011518770.1:p.Leu354=
XM_011520470.2:c.954T= XP_011518772.1:p.Leu318=
XM_017018540.2:c.1041T= XP_016874029.1:p.Leu347=
XM_017018541.2:c.933T= XP_016874030.1:p.Leu311=
XM_024448762.1:c.1191T= XP_024304530.1:p.Leu397=
XR_001748027.1:n.1262T=
XR_001748028.1:n.1244T=
XR_428862.3:n.1122T=
XR_428863.3:n.1118T=
XR_930928.2:n.1143T=
NM_001128225.3:c.1062T= MANE Select NP_001121697.2:p.Leu354=
NM_001330245.2:c.*59T= NP_001317174.2:n.*59T=
NM_152264.5:c.1041T= NP_689477.3:p.Leu347=