Canonical Allele Identifier: CA515260830
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51159406C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50720978C>G , CM000684.2:g.50720978C>G GRCh38
NC_000022.10:g.51159406C>G , CM000684.1:g.51159406C>G GRCh37
NC_000022.9:g.49506272C>G NCBI36
NG_008607.2:g.51624C>G
NG_070230.1:g.56762C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.2746C>G ENSP00000489147.2:p.Pro916Ala
ENST00000414786.7:n.3330C>G
ENST00000445220.7:c.1798C>G ENSP00000489407.2:p.Pro600Ala
ENST00000664402.2:c.1288C>G ENSP00000499475.1:p.Pro430Ala
ENST00000673971.2:c.*1744C>G ENSP00000501192.1:n.*1744C>G
ENST00000445220.6:c.1798C>G ENSP00000489407.2:p.Pro600Ala
ENST00000262795.6:c.2746C>G ENSP00000489147.2:p.Pro916Ala
ENST00000664402.1:c.1288C>G ENSP00000499475.1:p.Pro430Ala
ENST00000673971.1:c.*1744C>G ENSP00000501192.1:n.*1744C>G
ENST00000262795.5:c.3142C>G ENSP00000489147.1:p.Pro1048Ala
ENST00000414786.6:n.3330C>G
ENST00000445220.5:c.3124C>G ENSP00000489407.1:p.Pro1042Ala