Canonical Allele Identifier: CA380315125

Gene: SLC39A13

Linked Data

• MyVariant Identifiers: chr11:g.47436682C>T (hg19) ; chr11:g.47415131C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47415131C>T , CM000673.2:g.47415131C>T	GRCh38
NC_000011.9:g.47436682C>T , CM000673.1:g.47436682C>T	GRCh37
NC_000011.8:g.47393258C>T	NCBI36
NG_017073.1:g.11637C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362021.9:c.1012C>T MANE Select	ENSP00000354689.4:p.Pro338Ser
ENST00000354884.8:c.991C>T	ENSP00000346956.4:p.Pro331Ser
ENST00000362021.8:c.1012C>T	ENSP00000354689.4:p.Pro338Ser
ENST00000524886.1:n.270C>T
ENST00000524928.1:c.*1214C>T	ENSP00000437186.1:n.*1214C>T
ENST00000527829.1:n.244C>T
ENST00000533076.5:c.*9C>T	ENSP00000434290.1:n.*9C>T
NM_001128225.2:c.1012C>T	NP_001121697.1:p.Pro338Ser
NM_152264.4:c.991C>T	NP_689477.2:p.Pro331Ser
XM_006718381.2:c.1036C>T	XP_006718444.1:p.Pro346Ser
XM_006718383.2:c.928C>T	XP_006718446.1:p.Pro310Ser
XM_006718384.2:c.*9C>T	XP_006718447.1:n.*9C>T
XM_006718385.2:c.*9C>T	XP_006718448.1:n.*9C>T
XM_011520466.1:c.1057C>T	XP_011518768.1:p.Pro353Ser
XM_011520467.1:c.1012C>T	XP_011518769.1:p.Pro338Ser
XM_011520468.1:c.1012C>T	XP_011518770.1:p.Pro338Ser
XM_011520469.1:c.949C>T	XP_011518771.1:p.Pro317Ser
XM_011520470.1:c.904C>T	XP_011518772.1:p.Pro302Ser
XR_242832.1:n.1397C>T
XR_428862.2:n.1072C>T
XR_428863.2:n.1068C>T
XR_930928.1:n.1093C>T
NM_001330245.1:c.*9C>T	NP_001317174.1:n.*9C>T
NR_134854.1:n.1253C>T
XM_006718381.3:c.1036C>T	XP_006718444.1:p.Pro346Ser
XM_006718383.3:c.928C>T	XP_006718446.1:p.Pro310Ser
XM_011520468.3:c.1012C>T	XP_011518770.1:p.Pro338Ser
XM_011520470.2:c.904C>T	XP_011518772.1:p.Pro302Ser
XM_017018540.2:c.991C>T	XP_016874029.1:p.Pro331Ser
XM_017018541.2:c.883C>T	XP_016874030.1:p.Pro295Ser
XM_024448762.1:c.1141C>T	XP_024304530.1:p.Pro381Ser
XR_001748027.1:n.1212C>T
XR_001748028.1:n.1194C>T
XR_428862.3:n.1072C>T
XR_428863.3:n.1068C>T
XR_930928.2:n.1093C>T
NM_001128225.3:c.1012C>T MANE Select	NP_001121697.2:p.Pro338Ser
NM_001330245.2:c.*9C>T	NP_001317174.2:n.*9C>T
NM_152264.5:c.991C>T	NP_689477.3:p.Pro331Ser