Canonical Allele Identifier: CA515262077
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51159770C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50721342C>G , CM000684.2:g.50721342C>G GRCh38
NC_000022.10:g.51159770C>G , CM000684.1:g.51159770C>G GRCh37
NC_000022.9:g.49506636C>G NCBI36
NG_008607.2:g.51988C>G
NG_070230.1:g.57126C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.3110C>G ENSP00000489147.2:p.Pro1037Arg
ENST00000414786.7:n.3694C>G
ENST00000445220.7:c.2162C>G ENSP00000489407.2:p.Pro721Arg
ENST00000664402.2:c.1652C>G ENSP00000499475.1:p.Pro551Arg
ENST00000673971.2:c.*2108C>G ENSP00000501192.1:n.*2108C>G
ENST00000445220.6:c.2162C>G ENSP00000489407.2:p.Pro721Arg
ENST00000262795.6:c.3110C>G ENSP00000489147.2:p.Pro1037Arg
ENST00000664402.1:c.1652C>G ENSP00000499475.1:p.Pro551Arg
ENST00000673971.1:c.*2108C>G ENSP00000501192.1:n.*2108C>G
ENST00000262795.5:c.3506C>G ENSP00000489147.1:p.Pro1169Arg
ENST00000414786.6:n.3694C>G
ENST00000445220.5:c.3488C>G ENSP00000489407.1:p.Pro1163Arg