Canonical Allele Identifier: CA474210477

Gene: SLC39A13

Linked Data

• MyVariant Identifiers: chr11:g.47436881G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47415330G>T , CM000673.2:g.47415330G>T	GRCh38
NC_000011.9:g.47436881G>T , CM000673.1:g.47436881G>T	GRCh37
NC_000011.8:g.47393457G>T	NCBI36
NG_017073.1:g.11836G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362021.9:c.1083G>T MANE Select	ENSP00000354689.4:p.Val361=
ENST00000354884.8:c.1062G>T	ENSP00000346956.4:p.Val354=
ENST00000362021.8:c.1083G>T	ENSP00000354689.4:p.Val361=
ENST00000524886.1:n.341G>T
ENST00000524928.1:c.*1413G>T	ENSP00000437186.1:n.*1413G>T
ENST00000527829.1:n.443G>T
ENST00000533076.5:c.*80G>T	ENSP00000434290.1:n.*80G>T
NM_001128225.2:c.1083G>T	NP_001121697.1:p.Val361=
NM_152264.4:c.1062G>T	NP_689477.2:p.Val354=
XM_006718381.2:c.1107G>T	XP_006718444.1:p.Val369=
XM_006718383.2:c.999G>T	XP_006718446.1:p.Val333=
XM_006718384.2:c.*80G>T	XP_006718447.1:n.*80G>T
XM_006718385.2:c.*80G>T	XP_006718448.1:n.*80G>T
XM_011520466.1:c.1128G>T	XP_011518768.1:p.Val376=
XM_011520467.1:c.1083G>T	XP_011518769.1:p.Val361=
XM_011520468.1:c.1083G>T	XP_011518770.1:p.Val361=
XM_011520469.1:c.1020G>T	XP_011518771.1:p.Val340=
XM_011520470.1:c.975G>T	XP_011518772.1:p.Val325=
XR_242832.1:n.1468G>T
XR_428862.2:n.1143G>T
XR_428863.2:n.1139G>T
XR_930928.1:n.1164G>T
NM_001330245.1:c.*80G>T	NP_001317174.1:n.*80G>T
NR_134854.1:n.1324G>T
XM_006718381.3:c.1107G>T	XP_006718444.1:p.Val369=
XM_006718383.3:c.999G>T	XP_006718446.1:p.Val333=
XM_011520468.3:c.1083G>T	XP_011518770.1:p.Val361=
XM_011520470.2:c.975G>T	XP_011518772.1:p.Val325=
XM_017018540.2:c.1062G>T	XP_016874029.1:p.Val354=
XM_017018541.2:c.954G>T	XP_016874030.1:p.Val318=
XM_024448762.1:c.1212G>T	XP_024304530.1:p.Val404=
XR_001748027.1:n.1283G>T
XR_001748028.1:n.1265G>T
XR_428862.3:n.1143G>T
XR_428863.3:n.1139G>T
XR_930928.2:n.1164G>T
NM_001128225.3:c.1083G>T MANE Select	NP_001121697.2:p.Val361=
NM_001330245.2:c.*80G>T	NP_001317174.2:n.*80G>T
NM_152264.5:c.1062G>T	NP_689477.3:p.Val354=