Canonical Allele Identifier: CA515259807
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51159052T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50720624T>G , CM000684.2:g.50720624T>G GRCh38
NC_000022.10:g.51159052T>G , CM000684.1:g.51159052T>G GRCh37
NC_000022.9:g.49505918T>G NCBI36
NG_008607.2:g.51270T>G
NG_070230.1:g.56408T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.2392T>G ENSP00000489147.2:p.Tyr798Asp
ENST00000414786.7:n.2976T>G
ENST00000445220.7:c.1444T>G ENSP00000489407.2:p.Tyr482Asp
ENST00000664402.2:c.934T>G ENSP00000499475.1:p.Tyr312Asp
ENST00000673971.2:c.*1390T>G ENSP00000501192.1:n.*1390T>G
ENST00000445220.6:c.1444T>G ENSP00000489407.2:p.Tyr482Asp
ENST00000262795.6:c.2392T>G ENSP00000489147.2:p.Tyr798Asp
ENST00000664402.1:c.934T>G ENSP00000499475.1:p.Tyr312Asp
ENST00000673971.1:c.*1390T>G ENSP00000501192.1:n.*1390T>G
ENST00000262795.5:c.2788T>G ENSP00000489147.1:p.Tyr930Asp
ENST00000414786.6:n.2976T>G
ENST00000445220.5:c.2770T>G ENSP00000489407.1:p.Tyr924Asp