Canonical Allele Identifier: CA1969373841

Gene: SLC39A13

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47415292T= , CM000673.2:g.47415292T=	GRCh38
NC_000011.9:g.47436843T= , CM000673.1:g.47436843T=	GRCh37
NC_000011.8:g.47393419T=	NCBI36
NG_017073.1:g.11798T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362021.9:c.1045T= MANE Select	ENSP00000354689.4:p.Ser349=
ENST00000354884.8:c.1024T=	ENSP00000346956.4:p.Ser342=
ENST00000362021.8:c.1045T=	ENSP00000354689.4:p.Ser349=
ENST00000524886.1:n.303T=
ENST00000524928.1:c.*1375T=	ENSP00000437186.1:n.*1375T=
ENST00000527829.1:n.405T=
ENST00000533076.5:c.*42T=	ENSP00000434290.1:n.*42T=
NM_001128225.2:c.1045T=	NP_001121697.1:p.Ser349=
NM_152264.4:c.1024T=	NP_689477.2:p.Ser342=
XM_006718381.2:c.1069T=	XP_006718444.1:p.Ser357=
XM_006718383.2:c.961T=	XP_006718446.1:p.Ser321=
XM_006718384.2:c.*42T=	XP_006718447.1:n.*42T=
XM_006718385.2:c.*42T=	XP_006718448.1:n.*42T=
XM_011520466.1:c.1090T=	XP_011518768.1:p.Ser364=
XM_011520467.1:c.1045T=	XP_011518769.1:p.Ser349=
XM_011520468.1:c.1045T=	XP_011518770.1:p.Ser349=
XM_011520469.1:c.982T=	XP_011518771.1:p.Ser328=
XM_011520470.1:c.937T=	XP_011518772.1:p.Ser313=
XR_242832.1:n.1430T=
XR_428862.2:n.1105T=
XR_428863.2:n.1101T=
XR_930928.1:n.1126T=
NM_001330245.1:c.*42T=	NP_001317174.1:n.*42T=
NR_134854.1:n.1286T=
XM_006718381.3:c.1069T=	XP_006718444.1:p.Ser357=
XM_006718383.3:c.961T=	XP_006718446.1:p.Ser321=
XM_011520468.3:c.1045T=	XP_011518770.1:p.Ser349=
XM_011520470.2:c.937T=	XP_011518772.1:p.Ser313=
XM_017018540.2:c.1024T=	XP_016874029.1:p.Ser342=
XM_017018541.2:c.916T=	XP_016874030.1:p.Ser306=
XM_024448762.1:c.1174T=	XP_024304530.1:p.Ser392=
XR_001748027.1:n.1245T=
XR_001748028.1:n.1227T=
XR_428862.3:n.1105T=
XR_428863.3:n.1101T=
XR_930928.2:n.1126T=
NM_001128225.3:c.1045T= MANE Select	NP_001121697.2:p.Ser349=
NM_001330245.2:c.*42T=	NP_001317174.2:n.*42T=
NM_152264.5:c.1024T=	NP_689477.3:p.Ser342=