Canonical Allele Identifier: CA515264399
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51160517A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50722089A>C , CM000684.2:g.50722089A>C GRCh38
NC_000022.10:g.51160517A>C , CM000684.1:g.51160517A>C GRCh37
NC_000022.9:g.49507383A>C NCBI36
NG_008607.2:g.52735A>C
NG_070230.1:g.57873A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.3857A>C ENSP00000489147.2:p.Lys1286Thr
ENST00000414786.7:n.4441A>C
ENST00000445220.7:c.2909A>C ENSP00000489407.2:p.Lys970Thr
ENST00000664402.2:c.2399A>C ENSP00000499475.1:p.Lys800Thr
ENST00000673971.2:c.*2855A>C ENSP00000501192.1:n.*2855A>C
ENST00000445220.6:c.2909A>C ENSP00000489407.2:p.Lys970Thr
ENST00000262795.6:c.3857A>C ENSP00000489147.2:p.Lys1286Thr
ENST00000664402.1:c.2399A>C ENSP00000499475.1:p.Lys800Thr
ENST00000673971.1:c.*2855A>C ENSP00000501192.1:n.*2855A>C
ENST00000262795.5:c.4253A>C ENSP00000489147.1:p.Lys1418Thr
ENST00000414786.6:n.4441A>C
ENST00000445220.5:c.4235A>C ENSP00000489407.1:p.Lys1412Thr