Canonical Allele Identifier: CA515260716
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51159365T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50720937T>G , CM000684.2:g.50720937T>G GRCh38
NC_000022.10:g.51159365T>G , CM000684.1:g.51159365T>G GRCh37
NC_000022.9:g.49506231T>G NCBI36
NG_008607.2:g.51583T>G
NG_070230.1:g.56721T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.2705T>G ENSP00000489147.2:p.Ile902Ser
ENST00000414786.7:n.3289T>G
ENST00000445220.7:c.1757T>G ENSP00000489407.2:p.Ile586Ser
ENST00000664402.2:c.1247T>G ENSP00000499475.1:p.Ile416Ser
ENST00000673971.2:c.*1703T>G ENSP00000501192.1:n.*1703T>G
ENST00000445220.6:c.1757T>G ENSP00000489407.2:p.Ile586Ser
ENST00000262795.6:c.2705T>G ENSP00000489147.2:p.Ile902Ser
ENST00000664402.1:c.1247T>G ENSP00000499475.1:p.Ile416Ser
ENST00000673971.1:c.*1703T>G ENSP00000501192.1:n.*1703T>G
ENST00000262795.5:c.3101T>G ENSP00000489147.1:p.Ile1034Ser
ENST00000414786.6:n.3289T>G
ENST00000445220.5:c.3083T>G ENSP00000489407.1:p.Ile1028Ser