Canonical Allele Identifier: CA515260998
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51159469C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50721041C>T , CM000684.2:g.50721041C>T GRCh38
NC_000022.10:g.51159469C>T , CM000684.1:g.51159469C>T GRCh37
NC_000022.9:g.49506335C>T NCBI36
NG_008607.2:g.51687C>T
NG_070230.1:g.56825C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.2809C>T ENSP00000489147.2:p.Leu937=
ENST00000414786.7:n.3393C>T
ENST00000445220.7:c.1861C>T ENSP00000489407.2:p.Leu621=
ENST00000664402.2:c.1351C>T ENSP00000499475.1:p.Leu451=
ENST00000673971.2:c.*1807C>T ENSP00000501192.1:n.*1807C>T
ENST00000445220.6:c.1861C>T ENSP00000489407.2:p.Leu621=
ENST00000262795.6:c.2809C>T ENSP00000489147.2:p.Leu937=
ENST00000664402.1:c.1351C>T ENSP00000499475.1:p.Leu451=
ENST00000673971.1:c.*1807C>T ENSP00000501192.1:n.*1807C>T
ENST00000262795.5:c.3205C>T ENSP00000489147.1:p.Leu1069=
ENST00000414786.6:n.3393C>T
ENST00000445220.5:c.3187C>T ENSP00000489407.1:p.Leu1063=