Canonical Allele Identifier: CA515264805
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51160647C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50722219C>G , CM000684.2:g.50722219C>G GRCh38
NC_000022.10:g.51160647C>G , CM000684.1:g.51160647C>G GRCh37
NC_000022.9:g.49507513C>G NCBI36
NG_008607.2:g.52865C>G
NG_070230.1:g.58003C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.3987C>G ENSP00000489147.2:p.Arg1329=
ENST00000414786.7:n.4571C>G
ENST00000445220.7:c.3039C>G ENSP00000489407.2:p.Arg1013=
ENST00000664402.2:c.2529C>G ENSP00000499475.1:p.Arg843=
ENST00000673971.2:c.*2985C>G ENSP00000501192.1:n.*2985C>G
ENST00000445220.6:c.3039C>G ENSP00000489407.2:p.Arg1013=
ENST00000262795.6:c.3987C>G ENSP00000489147.2:p.Arg1329=
ENST00000664402.1:c.2529C>G ENSP00000499475.1:p.Arg843=
ENST00000673971.1:c.*2985C>G ENSP00000501192.1:n.*2985C>G
ENST00000262795.5:c.4383C>G ENSP00000489147.1:p.Arg1461=
ENST00000414786.6:n.4571C>G
ENST00000445220.5:c.4365C>G ENSP00000489407.1:p.Arg1455=