Canonical Allele Identifier: CA515258964
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51158762C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50720334C>G , CM000684.2:g.50720334C>G GRCh38
NC_000022.10:g.51158762C>G , CM000684.1:g.51158762C>G GRCh37
NC_000022.9:g.49505628C>G NCBI36
NG_008607.2:g.50980C>G
NG_070230.1:g.56118C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.2102C>G ENSP00000489147.2:p.Pro701Arg
ENST00000414786.7:n.2686C>G
ENST00000445220.7:c.1154C>G ENSP00000489407.2:p.Pro385Arg
ENST00000664402.2:c.644C>G ENSP00000499475.1:p.Pro215Arg
ENST00000673971.2:c.*1100C>G ENSP00000501192.1:n.*1100C>G
ENST00000445220.6:c.1154C>G ENSP00000489407.2:p.Pro385Arg
ENST00000262795.6:c.2102C>G ENSP00000489147.2:p.Pro701Arg
ENST00000664402.1:c.644C>G ENSP00000499475.1:p.Pro215Arg
ENST00000673971.1:c.*1100C>G ENSP00000501192.1:n.*1100C>G
ENST00000262795.5:c.2498C>G ENSP00000489147.1:p.Pro833Arg
ENST00000414786.6:n.2686C>G
ENST00000445220.5:c.2480C>G ENSP00000489407.1:p.Pro827Arg