Canonical Allele Identifier: CA515262776
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51159962C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50721534C>G , CM000684.2:g.50721534C>G GRCh38
NC_000022.10:g.51159962C>G , CM000684.1:g.51159962C>G GRCh37
NC_000022.9:g.49506828C>G NCBI36
NG_008607.2:g.52180C>G
NG_070230.1:g.57318C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.3302C>G ENSP00000489147.2:p.Thr1101Ser
ENST00000414786.7:n.3886C>G
ENST00000445220.7:c.2354C>G ENSP00000489407.2:p.Thr785Ser
ENST00000664402.2:c.1844C>G ENSP00000499475.1:p.Thr615Ser
ENST00000673971.2:c.*2300C>G ENSP00000501192.1:n.*2300C>G
ENST00000445220.6:c.2354C>G ENSP00000489407.2:p.Thr785Ser
ENST00000262795.6:c.3302C>G ENSP00000489147.2:p.Thr1101Ser
ENST00000664402.1:c.1844C>G ENSP00000499475.1:p.Thr615Ser
ENST00000673971.1:c.*2300C>G ENSP00000501192.1:n.*2300C>G
ENST00000262795.5:c.3698C>G ENSP00000489147.1:p.Thr1233Ser
ENST00000414786.6:n.3886C>G
ENST00000445220.5:c.3680C>G ENSP00000489407.1:p.Thr1227Ser