Canonical Allele Identifier: CA515262627
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51159921G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50721493G>C , CM000684.2:g.50721493G>C GRCh38
NC_000022.10:g.51159921G>C , CM000684.1:g.51159921G>C GRCh37
NC_000022.9:g.49506787G>C NCBI36
NG_008607.2:g.52139G>C
NG_070230.1:g.57277G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.3261G>C ENSP00000489147.2:p.Glu1087Asp
ENST00000414786.7:n.3845G>C
ENST00000445220.7:c.2313G>C ENSP00000489407.2:p.Glu771Asp
ENST00000664402.2:c.1803G>C ENSP00000499475.1:p.Glu601Asp
ENST00000673971.2:c.*2259G>C ENSP00000501192.1:n.*2259G>C
ENST00000445220.6:c.2313G>C ENSP00000489407.2:p.Glu771Asp
ENST00000262795.6:c.3261G>C ENSP00000489147.2:p.Glu1087Asp
ENST00000664402.1:c.1803G>C ENSP00000499475.1:p.Glu601Asp
ENST00000673971.1:c.*2259G>C ENSP00000501192.1:n.*2259G>C
ENST00000262795.5:c.3657G>C ENSP00000489147.1:p.Glu1219Asp
ENST00000414786.6:n.3845G>C
ENST00000445220.5:c.3639G>C ENSP00000489407.1:p.Glu1213Asp