Canonical Allele Identifier: CA515264631
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51160594C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50722166C>G , CM000684.2:g.50722166C>G GRCh38
NC_000022.10:g.51160594C>G , CM000684.1:g.51160594C>G GRCh37
NC_000022.9:g.49507460C>G NCBI36
NG_008607.2:g.52812C>G
NG_070230.1:g.57950C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.3934C>G ENSP00000489147.2:p.Gln1312Glu
ENST00000414786.7:n.4518C>G
ENST00000445220.7:c.2986C>G ENSP00000489407.2:p.Gln996Glu
ENST00000664402.2:c.2476C>G ENSP00000499475.1:p.Gln826Glu
ENST00000673971.2:c.*2932C>G ENSP00000501192.1:n.*2932C>G
ENST00000445220.6:c.2986C>G ENSP00000489407.2:p.Gln996Glu
ENST00000262795.6:c.3934C>G ENSP00000489147.2:p.Gln1312Glu
ENST00000664402.1:c.2476C>G ENSP00000499475.1:p.Gln826Glu
ENST00000673971.1:c.*2932C>G ENSP00000501192.1:n.*2932C>G
ENST00000262795.5:c.4330C>G ENSP00000489147.1:p.Gln1444Glu
ENST00000414786.6:n.4518C>G
ENST00000445220.5:c.4312C>G ENSP00000489407.1:p.Gln1438Glu