Canonical Allele Identifier: CA515264345
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51160498C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50722070C>G , CM000684.2:g.50722070C>G GRCh38
NC_000022.10:g.51160498C>G , CM000684.1:g.51160498C>G GRCh37
NC_000022.9:g.49507364C>G NCBI36
NG_008607.2:g.52716C>G
NG_070230.1:g.57854C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.3838C>G ENSP00000489147.2:p.Pro1280Ala
ENST00000414786.7:n.4422C>G
ENST00000445220.7:c.2890C>G ENSP00000489407.2:p.Pro964Ala
ENST00000664402.2:c.2380C>G ENSP00000499475.1:p.Pro794Ala
ENST00000673971.2:c.*2836C>G ENSP00000501192.1:n.*2836C>G
ENST00000445220.6:c.2890C>G ENSP00000489407.2:p.Pro964Ala
ENST00000262795.6:c.3838C>G ENSP00000489147.2:p.Pro1280Ala
ENST00000664402.1:c.2380C>G ENSP00000499475.1:p.Pro794Ala
ENST00000673971.1:c.*2836C>G ENSP00000501192.1:n.*2836C>G
ENST00000262795.5:c.4234C>G ENSP00000489147.1:p.Pro1412Ala
ENST00000414786.6:n.4422C>G
ENST00000445220.5:c.4216C>G ENSP00000489407.1:p.Pro1406Ala