Canonical Allele Identifier: CA515261122
Gene: SHANK3 HGNC NCBI

Linked Data

dbSNP Id: rs1348859127
MyVariant Identifiers: chr22:g.51159515G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50721087G>A , CM000684.2:g.50721087G>A GRCh38
NC_000022.10:g.51159515G>A , CM000684.1:g.51159515G>A GRCh37
NC_000022.9:g.49506381G>A NCBI36
NG_008607.2:g.51733G>A
NG_070230.1:g.56871G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.2855G>A ENSP00000489147.2:p.Ser952Asn
ENST00000414786.7:n.3439G>A
ENST00000445220.7:c.1907G>A ENSP00000489407.2:p.Ser636Asn
ENST00000664402.2:c.1397G>A ENSP00000499475.1:p.Ser466Asn
ENST00000673971.2:c.*1853G>A ENSP00000501192.1:n.*1853G>A
ENST00000445220.6:c.1907G>A ENSP00000489407.2:p.Ser636Asn
ENST00000262795.6:c.2855G>A ENSP00000489147.2:p.Ser952Asn
ENST00000664402.1:c.1397G>A ENSP00000499475.1:p.Ser466Asn
ENST00000673971.1:c.*1853G>A ENSP00000501192.1:n.*1853G>A
ENST00000262795.5:c.3251G>A ENSP00000489147.1:p.Ser1084Asn
ENST00000414786.6:n.3439G>A
ENST00000445220.5:c.3233G>A ENSP00000489407.1:p.Ser1078Asn