Canonical Allele Identifier: CA474210411

Gene: SLC39A13

Linked Data

• MyVariant Identifiers: chr11:g.47436708G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47415157G>C , CM000673.2:g.47415157G>C	GRCh38
NC_000011.9:g.47436708G>C , CM000673.1:g.47436708G>C	GRCh37
NC_000011.8:g.47393284G>C	NCBI36
NG_017073.1:g.11663G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362021.9:c.1038G>C MANE Select	ENSP00000354689.4:p.Pro346=
ENST00000354884.8:c.1017G>C	ENSP00000346956.4:p.Pro339=
ENST00000362021.8:c.1038G>C	ENSP00000354689.4:p.Pro346=
ENST00000524886.1:n.296G>C
ENST00000524928.1:c.*1240G>C	ENSP00000437186.1:n.*1240G>C
ENST00000527829.1:n.270G>C
ENST00000533076.5:c.*35G>C	ENSP00000434290.1:n.*35G>C
NM_001128225.2:c.1038G>C	NP_001121697.1:p.Pro346=
NM_152264.4:c.1017G>C	NP_689477.2:p.Pro339=
XM_006718381.2:c.1062G>C	XP_006718444.1:p.Pro354=
XM_006718383.2:c.954G>C	XP_006718446.1:p.Pro318=
XM_006718384.2:c.*35G>C	XP_006718447.1:n.*35G>C
XM_006718385.2:c.*35G>C	XP_006718448.1:n.*35G>C
XM_011520466.1:c.1083G>C	XP_011518768.1:p.Pro361=
XM_011520467.1:c.1038G>C	XP_011518769.1:p.Pro346=
XM_011520468.1:c.1038G>C	XP_011518770.1:p.Pro346=
XM_011520469.1:c.975G>C	XP_011518771.1:p.Pro325=
XM_011520470.1:c.930G>C	XP_011518772.1:p.Pro310=
XR_242832.1:n.1423G>C
XR_428862.2:n.1098G>C
XR_428863.2:n.1094G>C
XR_930928.1:n.1119G>C
NM_001330245.1:c.*35G>C	NP_001317174.1:n.*35G>C
NR_134854.1:n.1279G>C
XM_006718381.3:c.1062G>C	XP_006718444.1:p.Pro354=
XM_006718383.3:c.954G>C	XP_006718446.1:p.Pro318=
XM_011520468.3:c.1038G>C	XP_011518770.1:p.Pro346=
XM_011520470.2:c.930G>C	XP_011518772.1:p.Pro310=
XM_017018540.2:c.1017G>C	XP_016874029.1:p.Pro339=
XM_017018541.2:c.909G>C	XP_016874030.1:p.Pro303=
XM_024448762.1:c.1167G>C	XP_024304530.1:p.Pro389=
XR_001748027.1:n.1238G>C
XR_001748028.1:n.1220G>C
XR_428862.3:n.1098G>C
XR_428863.3:n.1094G>C
XR_930928.2:n.1119G>C
NM_001128225.3:c.1038G>C MANE Select	NP_001121697.2:p.Pro346=
NM_001330245.2:c.*35G>C	NP_001317174.2:n.*35G>C
NM_152264.5:c.1017G>C	NP_689477.3:p.Pro339=