Canonical Allele Identifier: CA515261871
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51159765G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50721337G>A , CM000684.2:g.50721337G>A GRCh38
NC_000022.10:g.51159765G>A , CM000684.1:g.51159765G>A GRCh37
NC_000022.9:g.49506631G>A NCBI36
NG_008607.2:g.51983G>A
NG_070230.1:g.57121G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.3105G>A ENSP00000489147.2:p.Trp1035Ter
ENST00000414786.7:n.3689G>A
ENST00000445220.7:c.2157G>A ENSP00000489407.2:p.Trp719Ter
ENST00000664402.2:c.1647G>A ENSP00000499475.1:p.Trp549Ter
ENST00000673971.2:c.*2103G>A ENSP00000501192.1:n.*2103G>A
ENST00000445220.6:c.2157G>A ENSP00000489407.2:p.Trp719Ter
ENST00000262795.6:c.3105G>A ENSP00000489147.2:p.Trp1035Ter
ENST00000664402.1:c.1647G>A ENSP00000499475.1:p.Trp549Ter
ENST00000673971.1:c.*2103G>A ENSP00000501192.1:n.*2103G>A
ENST00000262795.5:c.3501G>A ENSP00000489147.1:p.Trp1167Ter
ENST00000414786.6:n.3689G>A
ENST00000445220.5:c.3483G>A ENSP00000489407.1:p.Trp1161Ter