Canonical Allele Identifier: CA515260062
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51159136C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50720708C>T , CM000684.2:g.50720708C>T GRCh38
NC_000022.10:g.51159136C>T , CM000684.1:g.51159136C>T GRCh37
NC_000022.9:g.49506002C>T NCBI36
NG_008607.2:g.51354C>T
NG_070230.1:g.56492C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.2476C>T ENSP00000489147.2:p.Gln826Ter
ENST00000414786.7:n.3060C>T
ENST00000445220.7:c.1528C>T ENSP00000489407.2:p.Gln510Ter
ENST00000664402.2:c.1018C>T ENSP00000499475.1:p.Gln340Ter
ENST00000673971.2:c.*1474C>T ENSP00000501192.1:n.*1474C>T
ENST00000445220.6:c.1528C>T ENSP00000489407.2:p.Gln510Ter
ENST00000262795.6:c.2476C>T ENSP00000489147.2:p.Gln826Ter
ENST00000664402.1:c.1018C>T ENSP00000499475.1:p.Gln340Ter
ENST00000673971.1:c.*1474C>T ENSP00000501192.1:n.*1474C>T
ENST00000262795.5:c.2872C>T ENSP00000489147.1:p.Gln958Ter
ENST00000414786.6:n.3060C>T
ENST00000445220.5:c.2854C>T ENSP00000489407.1:p.Gln952Ter