Canonical Allele Identifier: CA515264543
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51160565A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50722137A>C , CM000684.2:g.50722137A>C GRCh38
NC_000022.10:g.51160565A>C , CM000684.1:g.51160565A>C GRCh37
NC_000022.9:g.49507431A>C NCBI36
NG_008607.2:g.52783A>C
NG_070230.1:g.57921A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000262795.7:c.3905A>C ENSP00000489147.2:p.Lys1302Thr
ENST00000414786.7:n.4489A>C
ENST00000445220.7:c.2957A>C ENSP00000489407.2:p.Lys986Thr
ENST00000664402.2:c.2447A>C ENSP00000499475.1:p.Lys816Thr
ENST00000673971.2:c.*2903A>C ENSP00000501192.1:n.*2903A>C
ENST00000445220.6:c.2957A>C ENSP00000489407.2:p.Lys986Thr
ENST00000262795.6:c.3905A>C ENSP00000489147.2:p.Lys1302Thr
ENST00000664402.1:c.2447A>C ENSP00000499475.1:p.Lys816Thr
ENST00000673971.1:c.*2903A>C ENSP00000501192.1:n.*2903A>C
ENST00000262795.5:c.4301A>C ENSP00000489147.1:p.Lys1434Thr
ENST00000414786.6:n.4489A>C
ENST00000445220.5:c.4283A>C ENSP00000489407.1:p.Lys1428Thr