Canonical Allele Identifier: CA515264355
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51160501C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50722073C>T , CM000684.2:g.50722073C>T GRCh38
NC_000022.10:g.51160501C>T , CM000684.1:g.51160501C>T GRCh37
NC_000022.9:g.49507367C>T NCBI36
NG_008607.2:g.52719C>T
NG_070230.1:g.57857C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.3841C>T ENSP00000489147.2:p.Pro1281Ser
ENST00000414786.7:n.4425C>T
ENST00000445220.7:c.2893C>T ENSP00000489407.2:p.Pro965Ser
ENST00000664402.2:c.2383C>T ENSP00000499475.1:p.Pro795Ser
ENST00000673971.2:c.*2839C>T ENSP00000501192.1:n.*2839C>T
ENST00000445220.6:c.2893C>T ENSP00000489407.2:p.Pro965Ser
ENST00000262795.6:c.3841C>T ENSP00000489147.2:p.Pro1281Ser
ENST00000664402.1:c.2383C>T ENSP00000499475.1:p.Pro795Ser
ENST00000673971.1:c.*2839C>T ENSP00000501192.1:n.*2839C>T
ENST00000262795.5:c.4237C>T ENSP00000489147.1:p.Pro1413Ser
ENST00000414786.6:n.4425C>T
ENST00000445220.5:c.4219C>T ENSP00000489407.1:p.Pro1407Ser