Canonical Allele Identifier: CA515260669
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51159349C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50720921C>G , CM000684.2:g.50720921C>G GRCh38
NC_000022.10:g.51159349C>G , CM000684.1:g.51159349C>G GRCh37
NC_000022.9:g.49506215C>G NCBI36
NG_008607.2:g.51567C>G
NG_070230.1:g.56705C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.2689C>G ENSP00000489147.2:p.Leu897Val
ENST00000414786.7:n.3273C>G
ENST00000445220.7:c.1741C>G ENSP00000489407.2:p.Leu581Val
ENST00000664402.2:c.1231C>G ENSP00000499475.1:p.Leu411Val
ENST00000673971.2:c.*1687C>G ENSP00000501192.1:n.*1687C>G
ENST00000445220.6:c.1741C>G ENSP00000489407.2:p.Leu581Val
ENST00000262795.6:c.2689C>G ENSP00000489147.2:p.Leu897Val
ENST00000664402.1:c.1231C>G ENSP00000499475.1:p.Leu411Val
ENST00000673971.1:c.*1687C>G ENSP00000501192.1:n.*1687C>G
ENST00000262795.5:c.3085C>G ENSP00000489147.1:p.Leu1029Val
ENST00000414786.6:n.3273C>G
ENST00000445220.5:c.3067C>G ENSP00000489407.1:p.Leu1023Val