Canonical Allele Identifier: CA2613414124

Gene: SLC39A13

Linked Data

• gnomAD v4: 11-47415125-GTGCTCCCTGACCTCTTGGAAGAAGAGGACCCGTGGTGAGTGACCTGTTGGAGGAAGAGGACTGCCACTCACAGGGCCCTTAGGGGCTCAGGAGGGAAGGGCTCCTGGCCGCTGCC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47415133_47415247del , CM000673.2:g.47415133_47415247del	GRCh38
NC_000011.9:g.47436684_47436798del , CM000673.1:g.47436684_47436798del	GRCh37
NC_000011.8:g.47393260_47393374del	NCBI36
NG_017073.1:g.11639_11753del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362021.9:c.1014_1041-41del
ENST00000354884.8:c.993_1020-41del
ENST00000362021.8:c.1014_1041-41del
ENST00000524886.1:n.272_299-41del
ENST00000524928.1:c.*1216_*1330del	ENSP00000437186.1:n.*1216_*1330del
ENST00000527829.1:n.246_360del
ENST00000533076.5:c.*11_*38-41del
NM_001128225.2:c.1014_1041-41del
NM_152264.4:c.993_1020-41del
XM_006718381.2:c.1038_1065-41del
XM_006718383.2:c.930_957-41del
XM_006718384.2:c.*11_*38-41del
XM_006718385.2:c.*11_*38-41del
XM_011520466.1:c.1059_1086-41del
XM_011520467.1:c.1014_1041-41del
XM_011520468.1:c.1014_1041-41del
XM_011520469.1:c.951_978-41del
XM_011520470.1:c.906_933-41del
XR_242832.1:n.1399_1426-41del
XR_428862.2:n.1074_1101-41del
XR_428863.2:n.1070_1097-41del
XR_930928.1:n.1095_1122-41del
NM_001330245.1:c.*11_*38-41del
NR_134854.1:n.1255_1282-41del
XM_006718381.3:c.1038_1065-41del
XM_006718383.3:c.930_957-41del
XM_011520468.3:c.1014_1041-41del
XM_011520470.2:c.906_933-41del
XM_017018540.2:c.993_1020-41del
XM_017018541.2:c.885_912-41del
XM_024448762.1:c.1143_1170-41del
XR_001748027.1:n.1214_1241-41del
XR_001748028.1:n.1196_1223-41del
XR_428862.3:n.1074_1101-41del
XR_428863.3:n.1070_1097-41del
XR_930928.2:n.1095_1122-41del
NM_001128225.3:c.1014_1041-41del
NM_001330245.2:c.*11_*38-41del
NM_152264.5:c.993_1020-41del