Canonical Allele Identifier: CA380315454
Gene: SLC39A13 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47415314T>A , CM000673.2:g.47415314T>A GRCh38
NC_000011.9:g.47436865T>A , CM000673.1:g.47436865T>A GRCh37
NC_000011.8:g.47393441T>A NCBI36
NG_017073.1:g.11820T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000362021.9:c.1067T>A MANE Select ENSP00000354689.4:p.Leu356His
ENST00000354884.8:c.1046T>A ENSP00000346956.4:p.Leu349His
ENST00000362021.8:c.1067T>A ENSP00000354689.4:p.Leu356His
ENST00000524886.1:n.325T>A
ENST00000524928.1:c.*1397T>A ENSP00000437186.1:n.*1397T>A
ENST00000527829.1:n.427T>A
ENST00000533076.5:c.*64T>A ENSP00000434290.1:n.*64T>A
NM_001128225.2:c.1067T>A NP_001121697.1:p.Leu356His
NM_152264.4:c.1046T>A NP_689477.2:p.Leu349His
XM_006718381.2:c.1091T>A XP_006718444.1:p.Leu364His
XM_006718383.2:c.983T>A XP_006718446.1:p.Leu328His
XM_006718384.2:c.*64T>A XP_006718447.1:n.*64T>A
XM_006718385.2:c.*64T>A XP_006718448.1:n.*64T>A
XM_011520466.1:c.1112T>A XP_011518768.1:p.Leu371His
XM_011520467.1:c.1067T>A XP_011518769.1:p.Leu356His
XM_011520468.1:c.1067T>A XP_011518770.1:p.Leu356His
XM_011520469.1:c.1004T>A XP_011518771.1:p.Leu335His
XM_011520470.1:c.959T>A XP_011518772.1:p.Leu320His
XR_242832.1:n.1452T>A
XR_428862.2:n.1127T>A
XR_428863.2:n.1123T>A
XR_930928.1:n.1148T>A
NM_001330245.1:c.*64T>A NP_001317174.1:n.*64T>A
NR_134854.1:n.1308T>A
XM_006718381.3:c.1091T>A XP_006718444.1:p.Leu364His
XM_006718383.3:c.983T>A XP_006718446.1:p.Leu328His
XM_011520468.3:c.1067T>A XP_011518770.1:p.Leu356His
XM_011520470.2:c.959T>A XP_011518772.1:p.Leu320His
XM_017018540.2:c.1046T>A XP_016874029.1:p.Leu349His
XM_017018541.2:c.938T>A XP_016874030.1:p.Leu313His
XM_024448762.1:c.1196T>A XP_024304530.1:p.Leu399His
XR_001748027.1:n.1267T>A
XR_001748028.1:n.1249T>A
XR_428862.3:n.1127T>A
XR_428863.3:n.1123T>A
XR_930928.2:n.1148T>A
NM_001128225.3:c.1067T>A MANE Select NP_001121697.2:p.Leu356His
NM_001330245.2:c.*64T>A NP_001317174.2:n.*64T>A
NM_152264.5:c.1046T>A NP_689477.3:p.Leu349His