Canonical Allele Identifier: CA515261359
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51159600T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50721172T>A , CM000684.2:g.50721172T>A GRCh38
NC_000022.10:g.51159600T>A , CM000684.1:g.51159600T>A GRCh37
NC_000022.9:g.49506466T>A NCBI36
NG_008607.2:g.51818T>A
NG_070230.1:g.56956T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.2940T>A ENSP00000489147.2:p.Ala980=
ENST00000414786.7:n.3524T>A
ENST00000445220.7:c.1992T>A ENSP00000489407.2:p.Ala664=
ENST00000664402.2:c.1482T>A ENSP00000499475.1:p.Ala494=
ENST00000673971.2:c.*1938T>A ENSP00000501192.1:n.*1938T>A
ENST00000445220.6:c.1992T>A ENSP00000489407.2:p.Ala664=
ENST00000262795.6:c.2940T>A ENSP00000489147.2:p.Ala980=
ENST00000664402.1:c.1482T>A ENSP00000499475.1:p.Ala494=
ENST00000673971.1:c.*1938T>A ENSP00000501192.1:n.*1938T>A
ENST00000262795.5:c.3336T>A ENSP00000489147.1:p.Ala1112=
ENST00000414786.6:n.3524T>A
ENST00000445220.5:c.3318T>A ENSP00000489407.1:p.Ala1106=