Canonical Allele Identifier: CA380315171

Gene: SLC39A13

Linked Data

• MyVariant Identifiers: chr11:g.47436692T>A (hg19) ; chr11:g.47415141T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47415141T>A , CM000673.2:g.47415141T>A	GRCh38
NC_000011.9:g.47436692T>A , CM000673.1:g.47436692T>A	GRCh37
NC_000011.8:g.47393268T>A	NCBI36
NG_017073.1:g.11647T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362021.9:c.1022T>A MANE Select	ENSP00000354689.4:p.Leu341Ter
ENST00000354884.8:c.1001T>A	ENSP00000346956.4:p.Leu334Ter
ENST00000362021.8:c.1022T>A	ENSP00000354689.4:p.Leu341Ter
ENST00000524886.1:n.280T>A
ENST00000524928.1:c.*1224T>A	ENSP00000437186.1:n.*1224T>A
ENST00000527829.1:n.254T>A
ENST00000533076.5:c.*19T>A	ENSP00000434290.1:n.*19T>A
NM_001128225.2:c.1022T>A	NP_001121697.1:p.Leu341Ter
NM_152264.4:c.1001T>A	NP_689477.2:p.Leu334Ter
XM_006718381.2:c.1046T>A	XP_006718444.1:p.Leu349Ter
XM_006718383.2:c.938T>A	XP_006718446.1:p.Leu313Ter
XM_006718384.2:c.*19T>A	XP_006718447.1:n.*19T>A
XM_006718385.2:c.*19T>A	XP_006718448.1:n.*19T>A
XM_011520466.1:c.1067T>A	XP_011518768.1:p.Leu356Ter
XM_011520467.1:c.1022T>A	XP_011518769.1:p.Leu341Ter
XM_011520468.1:c.1022T>A	XP_011518770.1:p.Leu341Ter
XM_011520469.1:c.959T>A	XP_011518771.1:p.Leu320Ter
XM_011520470.1:c.914T>A	XP_011518772.1:p.Leu305Ter
XR_242832.1:n.1407T>A
XR_428862.2:n.1082T>A
XR_428863.2:n.1078T>A
XR_930928.1:n.1103T>A
NM_001330245.1:c.*19T>A	NP_001317174.1:n.*19T>A
NR_134854.1:n.1263T>A
XM_006718381.3:c.1046T>A	XP_006718444.1:p.Leu349Ter
XM_006718383.3:c.938T>A	XP_006718446.1:p.Leu313Ter
XM_011520468.3:c.1022T>A	XP_011518770.1:p.Leu341Ter
XM_011520470.2:c.914T>A	XP_011518772.1:p.Leu305Ter
XM_017018540.2:c.1001T>A	XP_016874029.1:p.Leu334Ter
XM_017018541.2:c.893T>A	XP_016874030.1:p.Leu298Ter
XM_024448762.1:c.1151T>A	XP_024304530.1:p.Leu384Ter
XR_001748027.1:n.1222T>A
XR_001748028.1:n.1204T>A
XR_428862.3:n.1082T>A
XR_428863.3:n.1078T>A
XR_930928.2:n.1103T>A
NM_001128225.3:c.1022T>A MANE Select	NP_001121697.2:p.Leu341Ter
NM_001330245.2:c.*19T>A	NP_001317174.2:n.*19T>A
NM_152264.5:c.1001T>A	NP_689477.3:p.Leu334Ter