Canonical Allele Identifier: CA515260803
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51159397T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50720969T>C , CM000684.2:g.50720969T>C GRCh38
NC_000022.10:g.51159397T>C , CM000684.1:g.51159397T>C GRCh37
NC_000022.9:g.49506263T>C NCBI36
NG_008607.2:g.51615T>C
NG_070230.1:g.56753T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.2737T>C ENSP00000489147.2:p.Ser913Pro
ENST00000414786.7:n.3321T>C
ENST00000445220.7:c.1789T>C ENSP00000489407.2:p.Ser597Pro
ENST00000664402.2:c.1279T>C ENSP00000499475.1:p.Ser427Pro
ENST00000673971.2:c.*1735T>C ENSP00000501192.1:n.*1735T>C
ENST00000445220.6:c.1789T>C ENSP00000489407.2:p.Ser597Pro
ENST00000262795.6:c.2737T>C ENSP00000489147.2:p.Ser913Pro
ENST00000664402.1:c.1279T>C ENSP00000499475.1:p.Ser427Pro
ENST00000673971.1:c.*1735T>C ENSP00000501192.1:n.*1735T>C
ENST00000262795.5:c.3133T>C ENSP00000489147.1:p.Ser1045Pro
ENST00000414786.6:n.3321T>C
ENST00000445220.5:c.3115T>C ENSP00000489407.1:p.Ser1039Pro