Canonical Allele Identifier: CA474210465

Gene: SLC39A13

Linked Data

• MyVariant Identifiers: chr11:g.47436866C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47415315C>T , CM000673.2:g.47415315C>T	GRCh38
NC_000011.9:g.47436866C>T , CM000673.1:g.47436866C>T	GRCh37
NC_000011.8:g.47393442C>T	NCBI36
NG_017073.1:g.11821C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362021.9:c.1068C>T MANE Select	ENSP00000354689.4:p.Leu356=
ENST00000354884.8:c.1047C>T	ENSP00000346956.4:p.Leu349=
ENST00000362021.8:c.1068C>T	ENSP00000354689.4:p.Leu356=
ENST00000524886.1:n.326C>T
ENST00000524928.1:c.*1398C>T	ENSP00000437186.1:n.*1398C>T
ENST00000527829.1:n.428C>T
ENST00000533076.5:c.*65C>T	ENSP00000434290.1:n.*65C>T
NM_001128225.2:c.1068C>T	NP_001121697.1:p.Leu356=
NM_152264.4:c.1047C>T	NP_689477.2:p.Leu349=
XM_006718381.2:c.1092C>T	XP_006718444.1:p.Leu364=
XM_006718383.2:c.984C>T	XP_006718446.1:p.Leu328=
XM_006718384.2:c.*65C>T	XP_006718447.1:n.*65C>T
XM_006718385.2:c.*65C>T	XP_006718448.1:n.*65C>T
XM_011520466.1:c.1113C>T	XP_011518768.1:p.Leu371=
XM_011520467.1:c.1068C>T	XP_011518769.1:p.Leu356=
XM_011520468.1:c.1068C>T	XP_011518770.1:p.Leu356=
XM_011520469.1:c.1005C>T	XP_011518771.1:p.Leu335=
XM_011520470.1:c.960C>T	XP_011518772.1:p.Leu320=
XR_242832.1:n.1453C>T
XR_428862.2:n.1128C>T
XR_428863.2:n.1124C>T
XR_930928.1:n.1149C>T
NM_001330245.1:c.*65C>T	NP_001317174.1:n.*65C>T
NR_134854.1:n.1309C>T
XM_006718381.3:c.1092C>T	XP_006718444.1:p.Leu364=
XM_006718383.3:c.984C>T	XP_006718446.1:p.Leu328=
XM_011520468.3:c.1068C>T	XP_011518770.1:p.Leu356=
XM_011520470.2:c.960C>T	XP_011518772.1:p.Leu320=
XM_017018540.2:c.1047C>T	XP_016874029.1:p.Leu349=
XM_017018541.2:c.939C>T	XP_016874030.1:p.Leu313=
XM_024448762.1:c.1197C>T	XP_024304530.1:p.Leu399=
XR_001748027.1:n.1268C>T
XR_001748028.1:n.1250C>T
XR_428862.3:n.1128C>T
XR_428863.3:n.1124C>T
XR_930928.2:n.1149C>T
NM_001128225.3:c.1068C>T MANE Select	NP_001121697.2:p.Leu356=
NM_001330245.2:c.*65C>T	NP_001317174.2:n.*65C>T
NM_152264.5:c.1047C>T	NP_689477.3:p.Leu349=