Canonical Allele Identifier: CA1969373784
Gene: SLC39A13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47415162G= , CM000673.2:g.47415162G= GRCh38
NC_000011.9:g.47436713G= , CM000673.1:g.47436713G= GRCh37
NC_000011.8:g.47393289G= NCBI36
NG_017073.1:g.11668G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000362021.9:c.1040+3G= MANE Select ENSP00000354689.4:n.1040+3G=
ENST00000354884.8:c.1019+3G= ENSP00000346956.4:n.1019+3G=
ENST00000362021.8:c.1040+3G= ENSP00000354689.4:n.1040+3G=
ENST00000524886.1:n.298+3G=
ENST00000524928.1:c.*1245G= ENSP00000437186.1:n.*1245G=
ENST00000527829.1:n.275G=
ENST00000533076.5:c.*37+3G= ENSP00000434290.1:n.*37+3G=
NM_001128225.2:c.1040+3G= NP_001121697.1:n.1040+3G=
NM_152264.4:c.1019+3G= NP_689477.2:n.1019+3G=
XM_006718381.2:c.1064+3G= XP_006718444.1:n.1064+3G=
XM_006718383.2:c.956+3G= XP_006718446.1:n.956+3G=
XM_006718384.2:c.*37+3G= XP_006718447.1:n.*37+3G=
XM_006718385.2:c.*37+3G= XP_006718448.1:n.*37+3G=
XM_011520466.1:c.1085+3G= XP_011518768.1:n.1085+3G=
XM_011520467.1:c.1040+3G= XP_011518769.1:n.1040+3G=
XM_011520468.1:c.1040+3G= XP_011518770.1:n.1040+3G=
XM_011520469.1:c.977+3G= XP_011518771.1:n.977+3G=
XM_011520470.1:c.932+3G= XP_011518772.1:n.932+3G=
XR_242832.1:n.1425+3G=
XR_428862.2:n.1100+3G=
XR_428863.2:n.1096+3G=
XR_930928.1:n.1121+3G=
NM_001330245.1:c.*37+3G= NP_001317174.1:n.*37+3G=
NR_134854.1:n.1281+3G=
XM_006718381.3:c.1064+3G= XP_006718444.1:n.1064+3G=
XM_006718383.3:c.956+3G= XP_006718446.1:n.956+3G=
XM_011520468.3:c.1040+3G= XP_011518770.1:n.1040+3G=
XM_011520470.2:c.932+3G= XP_011518772.1:n.932+3G=
XM_017018540.2:c.1019+3G= XP_016874029.1:n.1019+3G=
XM_017018541.2:c.911+3G= XP_016874030.1:n.911+3G=
XM_024448762.1:c.1169+3G= XP_024304530.1:n.1169+3G=
XR_001748027.1:n.1240+3G=
XR_001748028.1:n.1222+3G=
XR_428862.3:n.1100+3G=
XR_428863.3:n.1096+3G=
XR_930928.2:n.1121+3G=
NM_001128225.3:c.1040+3G= MANE Select NP_001121697.2:n.1040+3G=
NM_001330245.2:c.*37+3G= NP_001317174.2:n.*37+3G=
NM_152264.5:c.1019+3G= NP_689477.3:n.1019+3G=