Canonical Allele Identifier: CA380315550

Gene: SLC39A13

Linked Data

• MyVariant Identifiers: chr11:g.47436885A>G (hg19) ; chr11:g.47415334A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47415334A>G , CM000673.2:g.47415334A>G	GRCh38
NC_000011.9:g.47436885A>G , CM000673.1:g.47436885A>G	GRCh37
NC_000011.8:g.47393461A>G	NCBI36
NG_017073.1:g.11840A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000362021.9:c.1087A>G MANE Select	ENSP00000354689.4:p.Met363Val
ENST00000354884.8:c.1066A>G	ENSP00000346956.4:p.Met356Val
ENST00000362021.8:c.1087A>G	ENSP00000354689.4:p.Met363Val
ENST00000524886.1:n.345A>G
ENST00000524928.1:c.*1417A>G	ENSP00000437186.1:n.*1417A>G
ENST00000527829.1:n.447A>G
ENST00000533076.5:c.*84A>G	ENSP00000434290.1:n.*84A>G
NM_001128225.2:c.1087A>G	NP_001121697.1:p.Met363Val
NM_152264.4:c.1066A>G	NP_689477.2:p.Met356Val
XM_006718381.2:c.1111A>G	XP_006718444.1:p.Met371Val
XM_006718383.2:c.1003A>G	XP_006718446.1:p.Met335Val
XM_006718384.2:c.*84A>G	XP_006718447.1:n.*84A>G
XM_006718385.2:c.*84A>G	XP_006718448.1:n.*84A>G
XM_011520466.1:c.1132A>G	XP_011518768.1:p.Met378Val
XM_011520467.1:c.1087A>G	XP_011518769.1:p.Met363Val
XM_011520468.1:c.1087A>G	XP_011518770.1:p.Met363Val
XM_011520469.1:c.1024A>G	XP_011518771.1:p.Met342Val
XM_011520470.1:c.979A>G	XP_011518772.1:p.Met327Val
XR_242832.1:n.1472A>G
XR_428862.2:n.1147A>G
XR_428863.2:n.1143A>G
XR_930928.1:n.1168A>G
NM_001330245.1:c.*84A>G	NP_001317174.1:n.*84A>G
NR_134854.1:n.1328A>G
XM_006718381.3:c.1111A>G	XP_006718444.1:p.Met371Val
XM_006718383.3:c.1003A>G	XP_006718446.1:p.Met335Val
XM_011520468.3:c.1087A>G	XP_011518770.1:p.Met363Val
XM_011520470.2:c.979A>G	XP_011518772.1:p.Met327Val
XM_017018540.2:c.1066A>G	XP_016874029.1:p.Met356Val
XM_017018541.2:c.958A>G	XP_016874030.1:p.Met320Val
XM_024448762.1:c.1216A>G	XP_024304530.1:p.Met406Val
XR_001748027.1:n.1287A>G
XR_001748028.1:n.1269A>G
XR_428862.3:n.1147A>G
XR_428863.3:n.1143A>G
XR_930928.2:n.1168A>G
NM_001128225.3:c.1087A>G MANE Select	NP_001121697.2:p.Met363Val
NM_001330245.2:c.*84A>G	NP_001317174.2:n.*84A>G
NM_152264.5:c.1066A>G	NP_689477.3:p.Met356Val