Canonical Allele Identifier: CA515259758
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51159034C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50720606C>G , CM000684.2:g.50720606C>G GRCh38
NC_000022.10:g.51159034C>G , CM000684.1:g.51159034C>G GRCh37
NC_000022.9:g.49505900C>G NCBI36
NG_008607.2:g.51252C>G
NG_070230.1:g.56390C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.2374C>G ENSP00000489147.2:p.Pro792Ala
ENST00000414786.7:n.2958C>G
ENST00000445220.7:c.1426C>G ENSP00000489407.2:p.Pro476Ala
ENST00000664402.2:c.916C>G ENSP00000499475.1:p.Pro306Ala
ENST00000673971.2:c.*1372C>G ENSP00000501192.1:n.*1372C>G
ENST00000445220.6:c.1426C>G ENSP00000489407.2:p.Pro476Ala
ENST00000262795.6:c.2374C>G ENSP00000489147.2:p.Pro792Ala
ENST00000664402.1:c.916C>G ENSP00000499475.1:p.Pro306Ala
ENST00000673971.1:c.*1372C>G ENSP00000501192.1:n.*1372C>G
ENST00000262795.5:c.2770C>G ENSP00000489147.1:p.Pro924Ala
ENST00000414786.6:n.2958C>G
ENST00000445220.5:c.2752C>G ENSP00000489407.1:p.Pro918Ala