Canonical Allele Identifier: CA716383977
Gene: ADAMTSL3 HGNC NCBI

Linked Data

dbSNP Id: rs36062109

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.83853935_83853958del , CM000677.2:g.83853935_83853958del GRCh38
NC_000015.9:g.84522687_84522710del , CM000677.1:g.84522687_84522710del GRCh37
NC_000015.8:g.82313691_82313714del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000286744.10:c.728-4831_728-4808del MANE Select ENSP00000286744.5:n.728-4831_728-4808del
ENST00000286744.9:c.728-4831_728-4808del ENSP00000286744.5:n.728-4831_728-4808del
ENST00000561483.5:n.943-4831_943-4808del
ENST00000567476.1:c.728-4831_728-4808del ENSP00000456313.1:n.728-4831_728-4808del
ENST00000569510.5:n.943-4831_943-4808del
NM_001301110.1:c.728-4831_728-4808del NP_001288039.1:n.728-4831_728-4808del
NM_207517.2:c.728-4831_728-4808del NP_997400.2:n.728-4831_728-4808del
XM_011521821.1:c.808+4213_808+4236del XP_011520123.1:n.808+4213_808+4236del
XM_011521822.1:c.808+4213_808+4236del XP_011520124.1:n.808+4213_808+4236del
XM_011521823.1:c.808+4213_808+4236del XP_011520125.1:n.808+4213_808+4236del
XM_011521824.1:c.808+4213_808+4236del XP_011520126.1:n.808+4213_808+4236del
XM_011521825.1:c.808+4213_808+4236del XP_011520127.1:n.808+4213_808+4236del
XR_931873.1:n.841+4213_841+4236del
XM_011521822.2:c.808+4213_808+4236del XP_011520124.1:n.808+4213_808+4236del
XM_011521823.2:c.808+4213_808+4236del XP_011520125.1:n.808+4213_808+4236del
XM_011521824.2:c.808+4213_808+4236del XP_011520126.1:n.808+4213_808+4236del
XM_011521825.2:c.808+4213_808+4236del XP_011520127.1:n.808+4213_808+4236del
XM_017022434.1:c.808+4213_808+4236del XP_016877923.1:n.808+4213_808+4236del
XM_017022435.1:c.232+4213_232+4236del XP_016877924.1:n.232+4213_232+4236del
XM_024450000.1:c.808+4213_808+4236del XP_024305768.1:n.808+4213_808+4236del
XR_931873.2:n.1023+4213_1023+4236del
NM_207517.3:c.728-4831_728-4808del MANE Select NP_997400.2:n.728-4831_728-4808del
NM_001301110.2:c.728-4831_728-4808del NP_001288039.1:n.728-4831_728-4808del