Canonical Allele Identifier: CA474210405

Gene: SLC39A13

Linked Data

• MyVariant Identifiers: chr11:g.47436702G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47415151G>A , CM000673.2:g.47415151G>A	GRCh38
NC_000011.9:g.47436702G>A , CM000673.1:g.47436702G>A	GRCh37
NC_000011.8:g.47393278G>A	NCBI36
NG_017073.1:g.11657G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362021.9:c.1032G>A MANE Select	ENSP00000354689.4:p.Glu344=
ENST00000354884.8:c.1011G>A	ENSP00000346956.4:p.Glu337=
ENST00000362021.8:c.1032G>A	ENSP00000354689.4:p.Glu344=
ENST00000524886.1:n.290G>A
ENST00000524928.1:c.*1234G>A	ENSP00000437186.1:n.*1234G>A
ENST00000527829.1:n.264G>A
ENST00000533076.5:c.*29G>A	ENSP00000434290.1:n.*29G>A
NM_001128225.2:c.1032G>A	NP_001121697.1:p.Glu344=
NM_152264.4:c.1011G>A	NP_689477.2:p.Glu337=
XM_006718381.2:c.1056G>A	XP_006718444.1:p.Glu352=
XM_006718383.2:c.948G>A	XP_006718446.1:p.Glu316=
XM_006718384.2:c.*29G>A	XP_006718447.1:n.*29G>A
XM_006718385.2:c.*29G>A	XP_006718448.1:n.*29G>A
XM_011520466.1:c.1077G>A	XP_011518768.1:p.Glu359=
XM_011520467.1:c.1032G>A	XP_011518769.1:p.Glu344=
XM_011520468.1:c.1032G>A	XP_011518770.1:p.Glu344=
XM_011520469.1:c.969G>A	XP_011518771.1:p.Glu323=
XM_011520470.1:c.924G>A	XP_011518772.1:p.Glu308=
XR_242832.1:n.1417G>A
XR_428862.2:n.1092G>A
XR_428863.2:n.1088G>A
XR_930928.1:n.1113G>A
NM_001330245.1:c.*29G>A	NP_001317174.1:n.*29G>A
NR_134854.1:n.1273G>A
XM_006718381.3:c.1056G>A	XP_006718444.1:p.Glu352=
XM_006718383.3:c.948G>A	XP_006718446.1:p.Glu316=
XM_011520468.3:c.1032G>A	XP_011518770.1:p.Glu344=
XM_011520470.2:c.924G>A	XP_011518772.1:p.Glu308=
XM_017018540.2:c.1011G>A	XP_016874029.1:p.Glu337=
XM_017018541.2:c.903G>A	XP_016874030.1:p.Glu301=
XM_024448762.1:c.1161G>A	XP_024304530.1:p.Glu387=
XR_001748027.1:n.1232G>A
XR_001748028.1:n.1214G>A
XR_428862.3:n.1092G>A
XR_428863.3:n.1088G>A
XR_930928.2:n.1113G>A
NM_001128225.3:c.1032G>A MANE Select	NP_001121697.2:p.Glu344=
NM_001330245.2:c.*29G>A	NP_001317174.2:n.*29G>A
NM_152264.5:c.1011G>A	NP_689477.3:p.Glu337=