Canonical Allele Identifier: CA515261141
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51159522G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50721094G>C , CM000684.2:g.50721094G>C GRCh38
NC_000022.10:g.51159522G>C , CM000684.1:g.51159522G>C GRCh37
NC_000022.9:g.49506388G>C NCBI36
NG_008607.2:g.51740G>C
NG_070230.1:g.56878G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.2862G>C ENSP00000489147.2:p.Gly954=
ENST00000414786.7:n.3446G>C
ENST00000445220.7:c.1914G>C ENSP00000489407.2:p.Gly638=
ENST00000664402.2:c.1404G>C ENSP00000499475.1:p.Gly468=
ENST00000673971.2:c.*1860G>C ENSP00000501192.1:n.*1860G>C
ENST00000445220.6:c.1914G>C ENSP00000489407.2:p.Gly638=
ENST00000262795.6:c.2862G>C ENSP00000489147.2:p.Gly954=
ENST00000664402.1:c.1404G>C ENSP00000499475.1:p.Gly468=
ENST00000673971.1:c.*1860G>C ENSP00000501192.1:n.*1860G>C
ENST00000262795.5:c.3258G>C ENSP00000489147.1:p.Gly1086=
ENST00000414786.6:n.3446G>C
ENST00000445220.5:c.3240G>C ENSP00000489407.1:p.Gly1080=