Canonical Allele Identifier: CA380315546

Gene: SLC39A13

Linked Data

• MyVariant Identifiers: chr11:g.47436883T>G (hg19) ; chr11:g.47415332T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47415332T>G , CM000673.2:g.47415332T>G	GRCh38
NC_000011.9:g.47436883T>G , CM000673.1:g.47436883T>G	GRCh37
NC_000011.8:g.47393459T>G	NCBI36
NG_017073.1:g.11838T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362021.9:c.1085T>G MANE Select	ENSP00000354689.4:p.Val362Gly
ENST00000354884.8:c.1064T>G	ENSP00000346956.4:p.Val355Gly
ENST00000362021.8:c.1085T>G	ENSP00000354689.4:p.Val362Gly
ENST00000524886.1:n.343T>G
ENST00000524928.1:c.*1415T>G	ENSP00000437186.1:n.*1415T>G
ENST00000527829.1:n.445T>G
ENST00000533076.5:c.*82T>G	ENSP00000434290.1:n.*82T>G
NM_001128225.2:c.1085T>G	NP_001121697.1:p.Val362Gly
NM_152264.4:c.1064T>G	NP_689477.2:p.Val355Gly
XM_006718381.2:c.1109T>G	XP_006718444.1:p.Val370Gly
XM_006718383.2:c.1001T>G	XP_006718446.1:p.Val334Gly
XM_006718384.2:c.*82T>G	XP_006718447.1:n.*82T>G
XM_006718385.2:c.*82T>G	XP_006718448.1:n.*82T>G
XM_011520466.1:c.1130T>G	XP_011518768.1:p.Val377Gly
XM_011520467.1:c.1085T>G	XP_011518769.1:p.Val362Gly
XM_011520468.1:c.1085T>G	XP_011518770.1:p.Val362Gly
XM_011520469.1:c.1022T>G	XP_011518771.1:p.Val341Gly
XM_011520470.1:c.977T>G	XP_011518772.1:p.Val326Gly
XR_242832.1:n.1470T>G
XR_428862.2:n.1145T>G
XR_428863.2:n.1141T>G
XR_930928.1:n.1166T>G
NM_001330245.1:c.*82T>G	NP_001317174.1:n.*82T>G
NR_134854.1:n.1326T>G
XM_006718381.3:c.1109T>G	XP_006718444.1:p.Val370Gly
XM_006718383.3:c.1001T>G	XP_006718446.1:p.Val334Gly
XM_011520468.3:c.1085T>G	XP_011518770.1:p.Val362Gly
XM_011520470.2:c.977T>G	XP_011518772.1:p.Val326Gly
XM_017018540.2:c.1064T>G	XP_016874029.1:p.Val355Gly
XM_017018541.2:c.956T>G	XP_016874030.1:p.Val319Gly
XM_024448762.1:c.1214T>G	XP_024304530.1:p.Val405Gly
XR_001748027.1:n.1285T>G
XR_001748028.1:n.1267T>G
XR_428862.3:n.1145T>G
XR_428863.3:n.1141T>G
XR_930928.2:n.1166T>G
NM_001128225.3:c.1085T>G MANE Select	NP_001121697.2:p.Val362Gly
NM_001330245.2:c.*82T>G	NP_001317174.2:n.*82T>G
NM_152264.5:c.1064T>G	NP_689477.3:p.Val355Gly