Canonical Allele Identifier: CA1969373773

Gene: SLC39A13

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47415132C= , CM000673.2:g.47415132C=	GRCh38
NC_000011.9:g.47436683C= , CM000673.1:g.47436683C=	GRCh37
NC_000011.8:g.47393259C=	NCBI36
NG_017073.1:g.11638C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362021.9:c.1013C= MANE Select	ENSP00000354689.4:p.Pro338=
ENST00000354884.8:c.992C=	ENSP00000346956.4:p.Pro331=
ENST00000362021.8:c.1013C=	ENSP00000354689.4:p.Pro338=
ENST00000524886.1:n.271C=
ENST00000524928.1:c.*1215C=	ENSP00000437186.1:n.*1215C=
ENST00000527829.1:n.245C=
ENST00000533076.5:c.*10C=	ENSP00000434290.1:n.*10C=
NM_001128225.2:c.1013C=	NP_001121697.1:p.Pro338=
NM_152264.4:c.992C=	NP_689477.2:p.Pro331=
XM_006718381.2:c.1037C=	XP_006718444.1:p.Pro346=
XM_006718383.2:c.929C=	XP_006718446.1:p.Pro310=
XM_006718384.2:c.*10C=	XP_006718447.1:n.*10C=
XM_006718385.2:c.*10C=	XP_006718448.1:n.*10C=
XM_011520466.1:c.1058C=	XP_011518768.1:p.Pro353=
XM_011520467.1:c.1013C=	XP_011518769.1:p.Pro338=
XM_011520468.1:c.1013C=	XP_011518770.1:p.Pro338=
XM_011520469.1:c.950C=	XP_011518771.1:p.Pro317=
XM_011520470.1:c.905C=	XP_011518772.1:p.Pro302=
XR_242832.1:n.1398C=
XR_428862.2:n.1073C=
XR_428863.2:n.1069C=
XR_930928.1:n.1094C=
NM_001330245.1:c.*10C=	NP_001317174.1:n.*10C=
NR_134854.1:n.1254C=
XM_006718381.3:c.1037C=	XP_006718444.1:p.Pro346=
XM_006718383.3:c.929C=	XP_006718446.1:p.Pro310=
XM_011520468.3:c.1013C=	XP_011518770.1:p.Pro338=
XM_011520470.2:c.905C=	XP_011518772.1:p.Pro302=
XM_017018540.2:c.992C=	XP_016874029.1:p.Pro331=
XM_017018541.2:c.884C=	XP_016874030.1:p.Pro295=
XM_024448762.1:c.1142C=	XP_024304530.1:p.Pro381=
XR_001748027.1:n.1213C=
XR_001748028.1:n.1195C=
XR_428862.3:n.1073C=
XR_428863.3:n.1069C=
XR_930928.2:n.1094C=
NM_001128225.3:c.1013C= MANE Select	NP_001121697.2:p.Pro338=
NM_001330245.2:c.*10C=	NP_001317174.2:n.*10C=
NM_152264.5:c.992C=	NP_689477.3:p.Pro331=