Canonical Allele Identifier: CA515263136
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51160090C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50721662C>G , CM000684.2:g.50721662C>G GRCh38
NC_000022.10:g.51160090C>G , CM000684.1:g.51160090C>G GRCh37
NC_000022.9:g.49506956C>G NCBI36
NG_008607.2:g.52308C>G
NG_070230.1:g.57446C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.3430C>G ENSP00000489147.2:p.Pro1144Ala
ENST00000414786.7:n.4014C>G
ENST00000445220.7:c.2482C>G ENSP00000489407.2:p.Pro828Ala
ENST00000664402.2:c.1972C>G ENSP00000499475.1:p.Pro658Ala
ENST00000673971.2:c.*2428C>G ENSP00000501192.1:n.*2428C>G
ENST00000445220.6:c.2482C>G ENSP00000489407.2:p.Pro828Ala
ENST00000262795.6:c.3430C>G ENSP00000489147.2:p.Pro1144Ala
ENST00000664402.1:c.1972C>G ENSP00000499475.1:p.Pro658Ala
ENST00000673971.1:c.*2428C>G ENSP00000501192.1:n.*2428C>G
ENST00000262795.5:c.3826C>G ENSP00000489147.1:p.Pro1276Ala
ENST00000414786.6:n.4014C>G
ENST00000445220.5:c.3808C>G ENSP00000489407.1:p.Pro1270Ala