Canonical Allele Identifier: CA515261422
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51159624C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50721196C>G , CM000684.2:g.50721196C>G GRCh38
NC_000022.10:g.51159624C>G , CM000684.1:g.51159624C>G GRCh37
NC_000022.9:g.49506490C>G NCBI36
NG_008607.2:g.51842C>G
NG_070230.1:g.56980C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.2964C>G ENSP00000489147.2:p.Ser988=
ENST00000414786.7:n.3548C>G
ENST00000445220.7:c.2016C>G ENSP00000489407.2:p.Ser672=
ENST00000664402.2:c.1506C>G ENSP00000499475.1:p.Ser502=
ENST00000673971.2:c.*1962C>G ENSP00000501192.1:n.*1962C>G
ENST00000445220.6:c.2016C>G ENSP00000489407.2:p.Ser672=
ENST00000262795.6:c.2964C>G ENSP00000489147.2:p.Ser988=
ENST00000664402.1:c.1506C>G ENSP00000499475.1:p.Ser502=
ENST00000673971.1:c.*1962C>G ENSP00000501192.1:n.*1962C>G
ENST00000262795.5:c.3360C>G ENSP00000489147.1:p.Ser1120=
ENST00000414786.6:n.3548C>G
ENST00000445220.5:c.3342C>G ENSP00000489407.1:p.Ser1114=