Canonical Allele Identifier: CA515259932
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51159091C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50720663C>G , CM000684.2:g.50720663C>G GRCh38
NC_000022.10:g.51159091C>G , CM000684.1:g.51159091C>G GRCh37
NC_000022.9:g.49505957C>G NCBI36
NG_008607.2:g.51309C>G
NG_070230.1:g.56447C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.2431C>G ENSP00000489147.2:p.Pro811Ala
ENST00000414786.7:n.3015C>G
ENST00000445220.7:c.1483C>G ENSP00000489407.2:p.Pro495Ala
ENST00000664402.2:c.973C>G ENSP00000499475.1:p.Pro325Ala
ENST00000673971.2:c.*1429C>G ENSP00000501192.1:n.*1429C>G
ENST00000445220.6:c.1483C>G ENSP00000489407.2:p.Pro495Ala
ENST00000262795.6:c.2431C>G ENSP00000489147.2:p.Pro811Ala
ENST00000664402.1:c.973C>G ENSP00000499475.1:p.Pro325Ala
ENST00000673971.1:c.*1429C>G ENSP00000501192.1:n.*1429C>G
ENST00000262795.5:c.2827C>G ENSP00000489147.1:p.Pro943Ala
ENST00000414786.6:n.3015C>G
ENST00000445220.5:c.2809C>G ENSP00000489407.1:p.Pro937Ala