Canonical Allele Identifier: CA1969373838

Gene: SLC39A13

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47415288G= , CM000673.2:g.47415288G=	GRCh38
NC_000011.9:g.47436839G= , CM000673.1:g.47436839G=	GRCh37
NC_000011.8:g.47393415G=	NCBI36
NG_017073.1:g.11794G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362021.9:c.1041G= MANE Select	ENSP00000354689.4:p.Trp347=
ENST00000354884.8:c.1020G=	ENSP00000346956.4:p.Trp340=
ENST00000362021.8:c.1041G=	ENSP00000354689.4:p.Trp347=
ENST00000524886.1:n.299G=
ENST00000524928.1:c.*1371G=	ENSP00000437186.1:n.*1371G=
ENST00000527829.1:n.401G=
ENST00000533076.5:c.*38G=	ENSP00000434290.1:n.*38G=
NM_001128225.2:c.1041G=	NP_001121697.1:p.Trp347=
NM_152264.4:c.1020G=	NP_689477.2:p.Trp340=
XM_006718381.2:c.1065G=	XP_006718444.1:p.Trp355=
XM_006718383.2:c.957G=	XP_006718446.1:p.Trp319=
XM_006718384.2:c.*38G=	XP_006718447.1:n.*38G=
XM_006718385.2:c.*38G=	XP_006718448.1:n.*38G=
XM_011520466.1:c.1086G=	XP_011518768.1:p.Trp362=
XM_011520467.1:c.1041G=	XP_011518769.1:p.Trp347=
XM_011520468.1:c.1041G=	XP_011518770.1:p.Trp347=
XM_011520469.1:c.978G=	XP_011518771.1:p.Trp326=
XM_011520470.1:c.933G=	XP_011518772.1:p.Trp311=
XR_242832.1:n.1426G=
XR_428862.2:n.1101G=
XR_428863.2:n.1097G=
XR_930928.1:n.1122G=
NM_001330245.1:c.*38G=	NP_001317174.1:n.*38G=
NR_134854.1:n.1282G=
XM_006718381.3:c.1065G=	XP_006718444.1:p.Trp355=
XM_006718383.3:c.957G=	XP_006718446.1:p.Trp319=
XM_011520468.3:c.1041G=	XP_011518770.1:p.Trp347=
XM_011520470.2:c.933G=	XP_011518772.1:p.Trp311=
XM_017018540.2:c.1020G=	XP_016874029.1:p.Trp340=
XM_017018541.2:c.912G=	XP_016874030.1:p.Trp304=
XM_024448762.1:c.1170G=	XP_024304530.1:p.Trp390=
XR_001748027.1:n.1241G=
XR_001748028.1:n.1223G=
XR_428862.3:n.1101G=
XR_428863.3:n.1097G=
XR_930928.2:n.1122G=
NM_001128225.3:c.1041G= MANE Select	NP_001121697.2:p.Trp347=
NM_001330245.2:c.*38G=	NP_001317174.2:n.*38G=
NM_152264.5:c.1020G=	NP_689477.3:p.Trp340=