Canonical Allele Identifier: CA515259828
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51159059A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50720631A>C , CM000684.2:g.50720631A>C GRCh38
NC_000022.10:g.51159059A>C , CM000684.1:g.51159059A>C GRCh37
NC_000022.9:g.49505925A>C NCBI36
NG_008607.2:g.51277A>C
NG_070230.1:g.56415A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.2399A>C ENSP00000489147.2:p.Asn800Thr
ENST00000414786.7:n.2983A>C
ENST00000445220.7:c.1451A>C ENSP00000489407.2:p.Asn484Thr
ENST00000664402.2:c.941A>C ENSP00000499475.1:p.Asn314Thr
ENST00000673971.2:c.*1397A>C ENSP00000501192.1:n.*1397A>C
ENST00000445220.6:c.1451A>C ENSP00000489407.2:p.Asn484Thr
ENST00000262795.6:c.2399A>C ENSP00000489147.2:p.Asn800Thr
ENST00000664402.1:c.941A>C ENSP00000499475.1:p.Asn314Thr
ENST00000673971.1:c.*1397A>C ENSP00000501192.1:n.*1397A>C
ENST00000262795.5:c.2795A>C ENSP00000489147.1:p.Asn932Thr
ENST00000414786.6:n.2983A>C
ENST00000445220.5:c.2777A>C ENSP00000489407.1:p.Asn926Thr