Canonical Allele Identifier: CA515264938
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51160689C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50722261C>T , CM000684.2:g.50722261C>T GRCh38
NC_000022.10:g.51160689C>T , CM000684.1:g.51160689C>T GRCh37
NC_000022.9:g.49507555C>T NCBI36
NG_008607.2:g.52907C>T
NG_070230.1:g.58045C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.4029C>T ENSP00000489147.2:p.Asp1343=
ENST00000414786.7:n.4613C>T
ENST00000445220.7:c.3081C>T ENSP00000489407.2:p.Asp1027=
ENST00000664402.2:c.2571C>T ENSP00000499475.1:p.Asp857=
ENST00000673971.2:c.*3027C>T ENSP00000501192.1:n.*3027C>T
ENST00000445220.6:c.3081C>T ENSP00000489407.2:p.Asp1027=
ENST00000262795.6:c.4029C>T ENSP00000489147.2:p.Asp1343=
ENST00000664402.1:c.2571C>T ENSP00000499475.1:p.Asp857=
ENST00000673971.1:c.*3027C>T ENSP00000501192.1:n.*3027C>T
ENST00000262795.5:c.4425C>T ENSP00000489147.1:p.Asp1475=
ENST00000414786.6:n.4613C>T
ENST00000445220.5:c.4407C>T ENSP00000489407.1:p.Asp1469=