Canonical Allele Identifier: CA1969373844
Gene: SLC39A13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47415296T= , CM000673.2:g.47415296T= GRCh38
NC_000011.9:g.47436847T= , CM000673.1:g.47436847T= GRCh37
NC_000011.8:g.47393423T= NCBI36
NG_017073.1:g.11802T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000362021.9:c.1049T= MANE Select ENSP00000354689.4:p.Leu350=
ENST00000354884.8:c.1028T= ENSP00000346956.4:p.Leu343=
ENST00000362021.8:c.1049T= ENSP00000354689.4:p.Leu350=
ENST00000524886.1:n.307T=
ENST00000524928.1:c.*1379T= ENSP00000437186.1:n.*1379T=
ENST00000527829.1:n.409T=
ENST00000533076.5:c.*46T= ENSP00000434290.1:n.*46T=
NM_001128225.2:c.1049T= NP_001121697.1:p.Leu350=
NM_152264.4:c.1028T= NP_689477.2:p.Leu343=
XM_006718381.2:c.1073T= XP_006718444.1:p.Leu358=
XM_006718383.2:c.965T= XP_006718446.1:p.Leu322=
XM_006718384.2:c.*46T= XP_006718447.1:n.*46T=
XM_006718385.2:c.*46T= XP_006718448.1:n.*46T=
XM_011520466.1:c.1094T= XP_011518768.1:p.Leu365=
XM_011520467.1:c.1049T= XP_011518769.1:p.Leu350=
XM_011520468.1:c.1049T= XP_011518770.1:p.Leu350=
XM_011520469.1:c.986T= XP_011518771.1:p.Leu329=
XM_011520470.1:c.941T= XP_011518772.1:p.Leu314=
XR_242832.1:n.1434T=
XR_428862.2:n.1109T=
XR_428863.2:n.1105T=
XR_930928.1:n.1130T=
NM_001330245.1:c.*46T= NP_001317174.1:n.*46T=
NR_134854.1:n.1290T=
XM_006718381.3:c.1073T= XP_006718444.1:p.Leu358=
XM_006718383.3:c.965T= XP_006718446.1:p.Leu322=
XM_011520468.3:c.1049T= XP_011518770.1:p.Leu350=
XM_011520470.2:c.941T= XP_011518772.1:p.Leu314=
XM_017018540.2:c.1028T= XP_016874029.1:p.Leu343=
XM_017018541.2:c.920T= XP_016874030.1:p.Leu307=
XM_024448762.1:c.1178T= XP_024304530.1:p.Leu393=
XR_001748027.1:n.1249T=
XR_001748028.1:n.1231T=
XR_428862.3:n.1109T=
XR_428863.3:n.1105T=
XR_930928.2:n.1130T=
NM_001128225.3:c.1049T= MANE Select NP_001121697.2:p.Leu350=
NM_001330245.2:c.*46T= NP_001317174.2:n.*46T=
NM_152264.5:c.1028T= NP_689477.3:p.Leu343=