Canonical Allele Identifier: CA221691567

Gene: SLC39A13

Linked Data

• dbSNP Id: rs746465400
• MyVariant Identifiers: chr11:g.47436693_47436694insGAA (hg19) ; chr11:g.47415142_47415143insGAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47415148_47415150dup , CM000673.2:g.47415148_47415150dup	GRCh38
NC_000011.9:g.47436699_47436701dup , CM000673.1:g.47436699_47436701dup	GRCh37
NC_000011.8:g.47393275_47393277dup	NCBI36
NG_017073.1:g.11654_11656dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362021.9:c.1029_1031dup MANE Select	ENSP00000354689.4:p.Glu344_Asp345insGlu
ENST00000354884.8:c.1008_1010dup	ENSP00000346956.4:p.Glu337_Asp338insGlu
ENST00000362021.8:c.1029_1031dup	ENSP00000354689.4:p.Glu344_Asp345insGlu
ENST00000524886.1:n.287_289dup
ENST00000524928.1:c.*1231_*1233dup	ENSP00000437186.1:n.*1231_*1233dup
ENST00000527829.1:n.261_263dup
ENST00000533076.5:c.*26_*28dup	ENSP00000434290.1:n.*26_*28dup
NM_001128225.2:c.1029_1031dup	NP_001121697.1:p.Glu344_Asp345insGlu
NM_152264.4:c.1008_1010dup	NP_689477.2:p.Glu337_Asp338insGlu
XM_006718381.2:c.1053_1055dup	XP_006718444.1:p.Glu352_Asp353insGlu
XM_006718383.2:c.945_947dup	XP_006718446.1:p.Glu316_Asp317insGlu
XM_006718384.2:c.*26_*28dup	XP_006718447.1:n.*26_*28dup
XM_006718385.2:c.*26_*28dup	XP_006718448.1:n.*26_*28dup
XM_011520466.1:c.1074_1076dup	XP_011518768.1:p.Glu359_Asp360insGlu
XM_011520467.1:c.1029_1031dup	XP_011518769.1:p.Glu344_Asp345insGlu
XM_011520468.1:c.1029_1031dup	XP_011518770.1:p.Glu344_Asp345insGlu
XM_011520469.1:c.966_968dup	XP_011518771.1:p.Glu323_Asp324insGlu
XM_011520470.1:c.921_923dup	XP_011518772.1:p.Glu308_Asp309insGlu
XR_242832.1:n.1414_1416dup
XR_428862.2:n.1089_1091dup
XR_428863.2:n.1085_1087dup
XR_930928.1:n.1110_1112dup
NM_001330245.1:c.*26_*28dup	NP_001317174.1:n.*26_*28dup
NR_134854.1:n.1270_1272dup
XM_006718381.3:c.1053_1055dup	XP_006718444.1:p.Glu352_Asp353insGlu
XM_006718383.3:c.945_947dup	XP_006718446.1:p.Glu316_Asp317insGlu
XM_011520468.3:c.1029_1031dup	XP_011518770.1:p.Glu344_Asp345insGlu
XM_011520470.2:c.921_923dup	XP_011518772.1:p.Glu308_Asp309insGlu
XM_017018540.2:c.1008_1010dup	XP_016874029.1:p.Glu337_Asp338insGlu
XM_017018541.2:c.900_902dup	XP_016874030.1:p.Glu301_Asp302insGlu
XM_024448762.1:c.1158_1160dup	XP_024304530.1:p.Glu387_Asp388insGlu
XR_001748027.1:n.1229_1231dup
XR_001748028.1:n.1211_1213dup
XR_428862.3:n.1089_1091dup
XR_428863.3:n.1085_1087dup
XR_930928.2:n.1110_1112dup
NM_001128225.3:c.1029_1031dup MANE Select	NP_001121697.2:p.Glu344_Asp345insGlu
NM_001330245.2:c.*26_*28dup	NP_001317174.2:n.*26_*28dup
NM_152264.5:c.1008_1010dup	NP_689477.3:p.Glu337_Asp338insGlu