Canonical Allele Identifier: CA1969373848
Gene: SLC39A13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47415307C= , CM000673.2:g.47415307C= GRCh38
NC_000011.9:g.47436858C= , CM000673.1:g.47436858C= GRCh37
NC_000011.8:g.47393434C= NCBI36
NG_017073.1:g.11813C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000362021.9:c.1060C= MANE Select ENSP00000354689.4:p.Leu354=
ENST00000354884.8:c.1039C= ENSP00000346956.4:p.Leu347=
ENST00000362021.8:c.1060C= ENSP00000354689.4:p.Leu354=
ENST00000524886.1:n.318C=
ENST00000524928.1:c.*1390C= ENSP00000437186.1:n.*1390C=
ENST00000527829.1:n.420C=
ENST00000533076.5:c.*57C= ENSP00000434290.1:n.*57C=
NM_001128225.2:c.1060C= NP_001121697.1:p.Leu354=
NM_152264.4:c.1039C= NP_689477.2:p.Leu347=
XM_006718381.2:c.1084C= XP_006718444.1:p.Leu362=
XM_006718383.2:c.976C= XP_006718446.1:p.Leu326=
XM_006718384.2:c.*57C= XP_006718447.1:n.*57C=
XM_006718385.2:c.*57C= XP_006718448.1:n.*57C=
XM_011520466.1:c.1105C= XP_011518768.1:p.Leu369=
XM_011520467.1:c.1060C= XP_011518769.1:p.Leu354=
XM_011520468.1:c.1060C= XP_011518770.1:p.Leu354=
XM_011520469.1:c.997C= XP_011518771.1:p.Leu333=
XM_011520470.1:c.952C= XP_011518772.1:p.Leu318=
XR_242832.1:n.1445C=
XR_428862.2:n.1120C=
XR_428863.2:n.1116C=
XR_930928.1:n.1141C=
NM_001330245.1:c.*57C= NP_001317174.1:n.*57C=
NR_134854.1:n.1301C=
XM_006718381.3:c.1084C= XP_006718444.1:p.Leu362=
XM_006718383.3:c.976C= XP_006718446.1:p.Leu326=
XM_011520468.3:c.1060C= XP_011518770.1:p.Leu354=
XM_011520470.2:c.952C= XP_011518772.1:p.Leu318=
XM_017018540.2:c.1039C= XP_016874029.1:p.Leu347=
XM_017018541.2:c.931C= XP_016874030.1:p.Leu311=
XM_024448762.1:c.1189C= XP_024304530.1:p.Leu397=
XR_001748027.1:n.1260C=
XR_001748028.1:n.1242C=
XR_428862.3:n.1120C=
XR_428863.3:n.1116C=
XR_930928.2:n.1141C=
NM_001128225.3:c.1060C= MANE Select NP_001121697.2:p.Leu354=
NM_001330245.2:c.*57C= NP_001317174.2:n.*57C=
NM_152264.5:c.1039C= NP_689477.3:p.Leu347=