Canonical Allele Identifier: CA515261019
Gene: SHANK3 HGNC NCBI

Linked Data

dbSNP Id: rs760441941
MyVariant Identifiers: chr22:g.51159477C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50721049C>A , CM000684.2:g.50721049C>A GRCh38
NC_000022.10:g.51159477C>A , CM000684.1:g.51159477C>A GRCh37
NC_000022.9:g.49506343C>A NCBI36
NG_008607.2:g.51695C>A
NG_070230.1:g.56833C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.2817C>A ENSP00000489147.2:p.Ser939=
ENST00000414786.7:n.3401C>A
ENST00000445220.7:c.1869C>A ENSP00000489407.2:p.Ser623=
ENST00000664402.2:c.1359C>A ENSP00000499475.1:p.Ser453=
ENST00000673971.2:c.*1815C>A ENSP00000501192.1:n.*1815C>A
ENST00000445220.6:c.1869C>A ENSP00000489407.2:p.Ser623=
ENST00000262795.6:c.2817C>A ENSP00000489147.2:p.Ser939=
ENST00000664402.1:c.1359C>A ENSP00000499475.1:p.Ser453=
ENST00000673971.1:c.*1815C>A ENSP00000501192.1:n.*1815C>A
ENST00000262795.5:c.3213C>A ENSP00000489147.1:p.Ser1071=
ENST00000414786.6:n.3401C>A
ENST00000445220.5:c.3195C>A ENSP00000489407.1:p.Ser1065=