Canonical Allele Identifier: CA515260058
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51159135G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50720707G>C , CM000684.2:g.50720707G>C GRCh38
NC_000022.10:g.51159135G>C , CM000684.1:g.51159135G>C GRCh37
NC_000022.9:g.49506001G>C NCBI36
NG_008607.2:g.51353G>C
NG_070230.1:g.56491G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.2475G>C ENSP00000489147.2:p.Leu825=
ENST00000414786.7:n.3059G>C
ENST00000445220.7:c.1527G>C ENSP00000489407.2:p.Leu509=
ENST00000664402.2:c.1017G>C ENSP00000499475.1:p.Leu339=
ENST00000673971.2:c.*1473G>C ENSP00000501192.1:n.*1473G>C
ENST00000445220.6:c.1527G>C ENSP00000489407.2:p.Leu509=
ENST00000262795.6:c.2475G>C ENSP00000489147.2:p.Leu825=
ENST00000664402.1:c.1017G>C ENSP00000499475.1:p.Leu339=
ENST00000673971.1:c.*1473G>C ENSP00000501192.1:n.*1473G>C
ENST00000262795.5:c.2871G>C ENSP00000489147.1:p.Leu957=
ENST00000414786.6:n.3059G>C
ENST00000445220.5:c.2853G>C ENSP00000489407.1:p.Leu951=