Canonical Allele Identifier: CA515259257
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51158862T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50720434T>G , CM000684.2:g.50720434T>G GRCh38
NC_000022.10:g.51158862T>G , CM000684.1:g.51158862T>G GRCh37
NC_000022.9:g.49505728T>G NCBI36
NG_008607.2:g.51080T>G
NG_070230.1:g.56218T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000262795.7:c.2202T>G ENSP00000489147.2:p.Ala734=
ENST00000414786.7:n.2786T>G
ENST00000445220.7:c.1254T>G ENSP00000489407.2:p.Ala418=
ENST00000664402.2:c.744T>G ENSP00000499475.1:p.Ala248=
ENST00000673971.2:c.*1200T>G ENSP00000501192.1:n.*1200T>G
ENST00000445220.6:c.1254T>G ENSP00000489407.2:p.Ala418=
ENST00000262795.6:c.2202T>G ENSP00000489147.2:p.Ala734=
ENST00000664402.1:c.744T>G ENSP00000499475.1:p.Ala248=
ENST00000673971.1:c.*1200T>G ENSP00000501192.1:n.*1200T>G
ENST00000262795.5:c.2598T>G ENSP00000489147.1:p.Ala866=
ENST00000414786.6:n.2786T>G
ENST00000445220.5:c.2580T>G ENSP00000489407.1:p.Ala860=