Canonical Allele Identifier: CA380315376
Gene: SLC39A13 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47415298C>A , CM000673.2:g.47415298C>A GRCh38
NC_000011.9:g.47436849C>A , CM000673.1:g.47436849C>A GRCh37
NC_000011.8:g.47393425C>A NCBI36
NG_017073.1:g.11804C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000362021.9:c.1051C>A MANE Select ENSP00000354689.4:p.Gln351Lys
ENST00000354884.8:c.1030C>A ENSP00000346956.4:p.Gln344Lys
ENST00000362021.8:c.1051C>A ENSP00000354689.4:p.Gln351Lys
ENST00000524886.1:n.309C>A
ENST00000524928.1:c.*1381C>A ENSP00000437186.1:n.*1381C>A
ENST00000527829.1:n.411C>A
ENST00000533076.5:c.*48C>A ENSP00000434290.1:n.*48C>A
NM_001128225.2:c.1051C>A NP_001121697.1:p.Gln351Lys
NM_152264.4:c.1030C>A NP_689477.2:p.Gln344Lys
XM_006718381.2:c.1075C>A XP_006718444.1:p.Gln359Lys
XM_006718383.2:c.967C>A XP_006718446.1:p.Gln323Lys
XM_006718384.2:c.*48C>A XP_006718447.1:n.*48C>A
XM_006718385.2:c.*48C>A XP_006718448.1:n.*48C>A
XM_011520466.1:c.1096C>A XP_011518768.1:p.Gln366Lys
XM_011520467.1:c.1051C>A XP_011518769.1:p.Gln351Lys
XM_011520468.1:c.1051C>A XP_011518770.1:p.Gln351Lys
XM_011520469.1:c.988C>A XP_011518771.1:p.Gln330Lys
XM_011520470.1:c.943C>A XP_011518772.1:p.Gln315Lys
XR_242832.1:n.1436C>A
XR_428862.2:n.1111C>A
XR_428863.2:n.1107C>A
XR_930928.1:n.1132C>A
NM_001330245.1:c.*48C>A NP_001317174.1:n.*48C>A
NR_134854.1:n.1292C>A
XM_006718381.3:c.1075C>A XP_006718444.1:p.Gln359Lys
XM_006718383.3:c.967C>A XP_006718446.1:p.Gln323Lys
XM_011520468.3:c.1051C>A XP_011518770.1:p.Gln351Lys
XM_011520470.2:c.943C>A XP_011518772.1:p.Gln315Lys
XM_017018540.2:c.1030C>A XP_016874029.1:p.Gln344Lys
XM_017018541.2:c.922C>A XP_016874030.1:p.Gln308Lys
XM_024448762.1:c.1180C>A XP_024304530.1:p.Gln394Lys
XR_001748027.1:n.1251C>A
XR_001748028.1:n.1233C>A
XR_428862.3:n.1111C>A
XR_428863.3:n.1107C>A
XR_930928.2:n.1132C>A
NM_001128225.3:c.1051C>A MANE Select NP_001121697.2:p.Gln351Lys
NM_001330245.2:c.*48C>A NP_001317174.2:n.*48C>A
NM_152264.5:c.1030C>A NP_689477.3:p.Gln344Lys