Canonical Allele Identifier: CA679877914
Gene: SHANK2 HGNC NCBI

Linked Data

dbSNP Id: rs1282785658

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.71083302_71083313del , CM000673.2:g.71083302_71083313del GRCh38
NG_042866.1:g.146489_146500del

Transcript Alleles

HGVS Amino-acid change
ENST00000601538.6:c.913-8033_913-8022del MANE Select ENSP00000469689.2:n.913-8033_913-8022del
ENST00000458632.2:c.321-8033_321-8022del
ENST00000601538.5:c.913-8033_913-8022del ENSP00000469689.2:n.913-8033_913-8022del
ENST00000608988.5:c.*476-8033_*476-8022del ENSP00000476264.2:n.*476-8033_*476-8022de...
ENST00000618363.4:c.57-8033_57-8022del
NM_012309.4:c.913-8033_913-8022del NP_036441.2:n.913-8033_913-8022del
XM_005277930.2:c.913-8033_913-8022del XP_005277987.1:n.913-8033_913-8022del
XM_006718478.2:c.913-8033_913-8022del XP_006718541.1:n.913-8033_913-8022del
XM_011544854.1:c.913-8033_913-8022del XP_011543156.1:n.913-8033_913-8022del
XM_011544855.1:c.913-8033_913-8022del XP_011543157.1:n.913-8033_913-8022del
XM_011544856.1:c.913-8033_913-8022del XP_011543158.1:n.913-8033_913-8022del
XM_011544857.1:c.913-8033_913-8022del XP_011543159.1:n.913-8033_913-8022del
XM_011544858.1:c.913-8033_913-8022del XP_011543160.1:n.913-8033_913-8022del
XM_017017387.1:c.913-8033_913-8022del XP_016872876.1:n.913-8033_913-8022del
XM_017017388.1:c.913-8033_913-8022del XP_016872877.1:n.913-8033_913-8022del
XM_017017389.1:c.913-8033_913-8022del XP_016872878.1:n.913-8033_913-8022del
NM_012309.5:c.913-8033_913-8022del MANE Select NP_036441.2:n.913-8033_913-8022del