Canonical Allele Identifier: CA1969373780

Gene: SLC39A13

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47415154C= , CM000673.2:g.47415154C=	GRCh38
NC_000011.9:g.47436705C= , CM000673.1:g.47436705C=	GRCh37
NC_000011.8:g.47393281C=	NCBI36
NG_017073.1:g.11660C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362021.9:c.1035C= MANE Select	ENSP00000354689.4:p.Asp345=
ENST00000354884.8:c.1014C=	ENSP00000346956.4:p.Asp338=
ENST00000362021.8:c.1035C=	ENSP00000354689.4:p.Asp345=
ENST00000524886.1:n.293C=
ENST00000524928.1:c.*1237C=	ENSP00000437186.1:n.*1237C=
ENST00000527829.1:n.267C=
ENST00000533076.5:c.*32C=	ENSP00000434290.1:n.*32C=
NM_001128225.2:c.1035C=	NP_001121697.1:p.Asp345=
NM_152264.4:c.1014C=	NP_689477.2:p.Asp338=
XM_006718381.2:c.1059C=	XP_006718444.1:p.Asp353=
XM_006718383.2:c.951C=	XP_006718446.1:p.Asp317=
XM_006718384.2:c.*32C=	XP_006718447.1:n.*32C=
XM_006718385.2:c.*32C=	XP_006718448.1:n.*32C=
XM_011520466.1:c.1080C=	XP_011518768.1:p.Asp360=
XM_011520467.1:c.1035C=	XP_011518769.1:p.Asp345=
XM_011520468.1:c.1035C=	XP_011518770.1:p.Asp345=
XM_011520469.1:c.972C=	XP_011518771.1:p.Asp324=
XM_011520470.1:c.927C=	XP_011518772.1:p.Asp309=
XR_242832.1:n.1420C=
XR_428862.2:n.1095C=
XR_428863.2:n.1091C=
XR_930928.1:n.1116C=
NM_001330245.1:c.*32C=	NP_001317174.1:n.*32C=
NR_134854.1:n.1276C=
XM_006718381.3:c.1059C=	XP_006718444.1:p.Asp353=
XM_006718383.3:c.951C=	XP_006718446.1:p.Asp317=
XM_011520468.3:c.1035C=	XP_011518770.1:p.Asp345=
XM_011520470.2:c.927C=	XP_011518772.1:p.Asp309=
XM_017018540.2:c.1014C=	XP_016874029.1:p.Asp338=
XM_017018541.2:c.906C=	XP_016874030.1:p.Asp302=
XM_024448762.1:c.1164C=	XP_024304530.1:p.Asp388=
XR_001748027.1:n.1235C=
XR_001748028.1:n.1217C=
XR_428862.3:n.1095C=
XR_428863.3:n.1091C=
XR_930928.2:n.1116C=
NM_001128225.3:c.1035C= MANE Select	NP_001121697.2:p.Asp345=
NM_001330245.2:c.*32C=	NP_001317174.2:n.*32C=
NM_152264.5:c.1014C=	NP_689477.3:p.Asp338=