Canonical Allele Identifier: CA1969373839
Gene: SLC39A13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47415289C= , CM000673.2:g.47415289C= GRCh38
NC_000011.9:g.47436840C= , CM000673.1:g.47436840C= GRCh37
NC_000011.8:g.47393416C= NCBI36
NG_017073.1:g.11795C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000362021.9:c.1042C= MANE Select ENSP00000354689.4:p.Arg348=
ENST00000354884.8:c.1021C= ENSP00000346956.4:p.Arg341=
ENST00000362021.8:c.1042C= ENSP00000354689.4:p.Arg348=
ENST00000524886.1:n.300C=
ENST00000524928.1:c.*1372C= ENSP00000437186.1:n.*1372C=
ENST00000527829.1:n.402C=
ENST00000533076.5:c.*39C= ENSP00000434290.1:n.*39C=
NM_001128225.2:c.1042C= NP_001121697.1:p.Arg348=
NM_152264.4:c.1021C= NP_689477.2:p.Arg341=
XM_006718381.2:c.1066C= XP_006718444.1:p.Arg356=
XM_006718383.2:c.958C= XP_006718446.1:p.Arg320=
XM_006718384.2:c.*39C= XP_006718447.1:n.*39C=
XM_006718385.2:c.*39C= XP_006718448.1:n.*39C=
XM_011520466.1:c.1087C= XP_011518768.1:p.Arg363=
XM_011520467.1:c.1042C= XP_011518769.1:p.Arg348=
XM_011520468.1:c.1042C= XP_011518770.1:p.Arg348=
XM_011520469.1:c.979C= XP_011518771.1:p.Arg327=
XM_011520470.1:c.934C= XP_011518772.1:p.Arg312=
XR_242832.1:n.1427C=
XR_428862.2:n.1102C=
XR_428863.2:n.1098C=
XR_930928.1:n.1123C=
NM_001330245.1:c.*39C= NP_001317174.1:n.*39C=
NR_134854.1:n.1283C=
XM_006718381.3:c.1066C= XP_006718444.1:p.Arg356=
XM_006718383.3:c.958C= XP_006718446.1:p.Arg320=
XM_011520468.3:c.1042C= XP_011518770.1:p.Arg348=
XM_011520470.2:c.934C= XP_011518772.1:p.Arg312=
XM_017018540.2:c.1021C= XP_016874029.1:p.Arg341=
XM_017018541.2:c.913C= XP_016874030.1:p.Arg305=
XM_024448762.1:c.1171C= XP_024304530.1:p.Arg391=
XR_001748027.1:n.1242C=
XR_001748028.1:n.1224C=
XR_428862.3:n.1102C=
XR_428863.3:n.1098C=
XR_930928.2:n.1123C=
NM_001128225.3:c.1042C= MANE Select NP_001121697.2:p.Arg348=
NM_001330245.2:c.*39C= NP_001317174.2:n.*39C=
NM_152264.5:c.1021C= NP_689477.3:p.Arg341=