Canonical Allele Identifier: CA380315237

Gene: SLC39A13

Linked Data

• MyVariant Identifiers: chr11:g.47436704A>T (hg19) ; chr11:g.47415153A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47415153A>T , CM000673.2:g.47415153A>T	GRCh38
NC_000011.9:g.47436704A>T , CM000673.1:g.47436704A>T	GRCh37
NC_000011.8:g.47393280A>T	NCBI36
NG_017073.1:g.11659A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362021.9:c.1034A>T MANE Select	ENSP00000354689.4:p.Asp345Val
ENST00000354884.8:c.1013A>T	ENSP00000346956.4:p.Asp338Val
ENST00000362021.8:c.1034A>T	ENSP00000354689.4:p.Asp345Val
ENST00000524886.1:n.292A>T
ENST00000524928.1:c.*1236A>T	ENSP00000437186.1:n.*1236A>T
ENST00000527829.1:n.266A>T
ENST00000533076.5:c.*31A>T	ENSP00000434290.1:n.*31A>T
NM_001128225.2:c.1034A>T	NP_001121697.1:p.Asp345Val
NM_152264.4:c.1013A>T	NP_689477.2:p.Asp338Val
XM_006718381.2:c.1058A>T	XP_006718444.1:p.Asp353Val
XM_006718383.2:c.950A>T	XP_006718446.1:p.Asp317Val
XM_006718384.2:c.*31A>T	XP_006718447.1:n.*31A>T
XM_006718385.2:c.*31A>T	XP_006718448.1:n.*31A>T
XM_011520466.1:c.1079A>T	XP_011518768.1:p.Asp360Val
XM_011520467.1:c.1034A>T	XP_011518769.1:p.Asp345Val
XM_011520468.1:c.1034A>T	XP_011518770.1:p.Asp345Val
XM_011520469.1:c.971A>T	XP_011518771.1:p.Asp324Val
XM_011520470.1:c.926A>T	XP_011518772.1:p.Asp309Val
XR_242832.1:n.1419A>T
XR_428862.2:n.1094A>T
XR_428863.2:n.1090A>T
XR_930928.1:n.1115A>T
NM_001330245.1:c.*31A>T	NP_001317174.1:n.*31A>T
NR_134854.1:n.1275A>T
XM_006718381.3:c.1058A>T	XP_006718444.1:p.Asp353Val
XM_006718383.3:c.950A>T	XP_006718446.1:p.Asp317Val
XM_011520468.3:c.1034A>T	XP_011518770.1:p.Asp345Val
XM_011520470.2:c.926A>T	XP_011518772.1:p.Asp309Val
XM_017018540.2:c.1013A>T	XP_016874029.1:p.Asp338Val
XM_017018541.2:c.905A>T	XP_016874030.1:p.Asp302Val
XM_024448762.1:c.1163A>T	XP_024304530.1:p.Asp388Val
XR_001748027.1:n.1234A>T
XR_001748028.1:n.1216A>T
XR_428862.3:n.1094A>T
XR_428863.3:n.1090A>T
XR_930928.2:n.1115A>T
NM_001128225.3:c.1034A>T MANE Select	NP_001121697.2:p.Asp345Val
NM_001330245.2:c.*31A>T	NP_001317174.2:n.*31A>T
NM_152264.5:c.1013A>T	NP_689477.3:p.Asp338Val