Canonical Allele Identifier: CA515261132
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51159519G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50721091G>A , CM000684.2:g.50721091G>A GRCh38
NC_000022.10:g.51159519G>A , CM000684.1:g.51159519G>A GRCh37
NC_000022.9:g.49506385G>A NCBI36
NG_008607.2:g.51737G>A
NG_070230.1:g.56875G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.2859G>A ENSP00000489147.2:p.Leu953=
ENST00000414786.7:n.3443G>A
ENST00000445220.7:c.1911G>A ENSP00000489407.2:p.Leu637=
ENST00000664402.2:c.1401G>A ENSP00000499475.1:p.Leu467=
ENST00000673971.2:c.*1857G>A ENSP00000501192.1:n.*1857G>A
ENST00000445220.6:c.1911G>A ENSP00000489407.2:p.Leu637=
ENST00000262795.6:c.2859G>A ENSP00000489147.2:p.Leu953=
ENST00000664402.1:c.1401G>A ENSP00000499475.1:p.Leu467=
ENST00000673971.1:c.*1857G>A ENSP00000501192.1:n.*1857G>A
ENST00000262795.5:c.3255G>A ENSP00000489147.1:p.Leu1085=
ENST00000414786.6:n.3443G>A
ENST00000445220.5:c.3237G>A ENSP00000489407.1:p.Leu1079=