Canonical Allele Identifier: CA515262708
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51159942C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50721514C>A , CM000684.2:g.50721514C>A GRCh38
NC_000022.10:g.51159942C>A , CM000684.1:g.51159942C>A GRCh37
NC_000022.9:g.49506808C>A NCBI36
NG_008607.2:g.52160C>A
NG_070230.1:g.57298C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.3282C>A ENSP00000489147.2:p.Ala1094=
ENST00000414786.7:n.3866C>A
ENST00000445220.7:c.2334C>A ENSP00000489407.2:p.Ala778=
ENST00000664402.2:c.1824C>A ENSP00000499475.1:p.Ala608=
ENST00000673971.2:c.*2280C>A ENSP00000501192.1:n.*2280C>A
ENST00000445220.6:c.2334C>A ENSP00000489407.2:p.Ala778=
ENST00000262795.6:c.3282C>A ENSP00000489147.2:p.Ala1094=
ENST00000664402.1:c.1824C>A ENSP00000499475.1:p.Ala608=
ENST00000673971.1:c.*2280C>A ENSP00000501192.1:n.*2280C>A
ENST00000262795.5:c.3678C>A ENSP00000489147.1:p.Ala1226=
ENST00000414786.6:n.3866C>A
ENST00000445220.5:c.3660C>A ENSP00000489407.1:p.Ala1220=