Canonical Allele Identifier: CA380315166
Gene: SLC39A13 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47415140T>A , CM000673.2:g.47415140T>A GRCh38
NC_000011.9:g.47436691T>A , CM000673.1:g.47436691T>A GRCh37
NC_000011.8:g.47393267T>A NCBI36
NG_017073.1:g.11646T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000362021.9:c.1021T>A MANE Select ENSP00000354689.4:p.Leu341Met
ENST00000354884.8:c.1000T>A ENSP00000346956.4:p.Leu334Met
ENST00000362021.8:c.1021T>A ENSP00000354689.4:p.Leu341Met
ENST00000524886.1:n.279T>A
ENST00000524928.1:c.*1223T>A ENSP00000437186.1:n.*1223T>A
ENST00000527829.1:n.253T>A
ENST00000533076.5:c.*18T>A ENSP00000434290.1:n.*18T>A
NM_001128225.2:c.1021T>A NP_001121697.1:p.Leu341Met
NM_152264.4:c.1000T>A NP_689477.2:p.Leu334Met
XM_006718381.2:c.1045T>A XP_006718444.1:p.Leu349Met
XM_006718383.2:c.937T>A XP_006718446.1:p.Leu313Met
XM_006718384.2:c.*18T>A XP_006718447.1:n.*18T>A
XM_006718385.2:c.*18T>A XP_006718448.1:n.*18T>A
XM_011520466.1:c.1066T>A XP_011518768.1:p.Leu356Met
XM_011520467.1:c.1021T>A XP_011518769.1:p.Leu341Met
XM_011520468.1:c.1021T>A XP_011518770.1:p.Leu341Met
XM_011520469.1:c.958T>A XP_011518771.1:p.Leu320Met
XM_011520470.1:c.913T>A XP_011518772.1:p.Leu305Met
XR_242832.1:n.1406T>A
XR_428862.2:n.1081T>A
XR_428863.2:n.1077T>A
XR_930928.1:n.1102T>A
NM_001330245.1:c.*18T>A NP_001317174.1:n.*18T>A
NR_134854.1:n.1262T>A
XM_006718381.3:c.1045T>A XP_006718444.1:p.Leu349Met
XM_006718383.3:c.937T>A XP_006718446.1:p.Leu313Met
XM_011520468.3:c.1021T>A XP_011518770.1:p.Leu341Met
XM_011520470.2:c.913T>A XP_011518772.1:p.Leu305Met
XM_017018540.2:c.1000T>A XP_016874029.1:p.Leu334Met
XM_017018541.2:c.892T>A XP_016874030.1:p.Leu298Met
XM_024448762.1:c.1150T>A XP_024304530.1:p.Leu384Met
XR_001748027.1:n.1221T>A
XR_001748028.1:n.1203T>A
XR_428862.3:n.1081T>A
XR_428863.3:n.1077T>A
XR_930928.2:n.1102T>A
NM_001128225.3:c.1021T>A MANE Select NP_001121697.2:p.Leu341Met
NM_001330245.2:c.*18T>A NP_001317174.2:n.*18T>A
NM_152264.5:c.1000T>A NP_689477.3:p.Leu334Met