Canonical Allele Identifier: CA515262874
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51159993A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50721565A>G , CM000684.2:g.50721565A>G GRCh38
NC_000022.10:g.51159993A>G , CM000684.1:g.51159993A>G GRCh37
NC_000022.9:g.49506859A>G NCBI36
NG_008607.2:g.52211A>G
NG_070230.1:g.57349A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.3333A>G ENSP00000489147.2:p.Ser1111=
ENST00000414786.7:n.3917A>G
ENST00000445220.7:c.2385A>G ENSP00000489407.2:p.Ser795=
ENST00000664402.2:c.1875A>G ENSP00000499475.1:p.Ser625=
ENST00000673971.2:c.*2331A>G ENSP00000501192.1:n.*2331A>G
ENST00000445220.6:c.2385A>G ENSP00000489407.2:p.Ser795=
ENST00000262795.6:c.3333A>G ENSP00000489147.2:p.Ser1111=
ENST00000664402.1:c.1875A>G ENSP00000499475.1:p.Ser625=
ENST00000673971.1:c.*2331A>G ENSP00000501192.1:n.*2331A>G
ENST00000262795.5:c.3729A>G ENSP00000489147.1:p.Ser1243=
ENST00000414786.6:n.3917A>G
ENST00000445220.5:c.3711A>G ENSP00000489407.1:p.Ser1237=