Canonical Allele Identifier: CA515261629
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51159703G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50721275G>C , CM000684.2:g.50721275G>C GRCh38
NC_000022.10:g.51159703G>C , CM000684.1:g.51159703G>C GRCh37
NC_000022.9:g.49506569G>C NCBI36
NG_008607.2:g.51921G>C
NG_070230.1:g.57059G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.3043G>C ENSP00000489147.2:p.Ala1015Pro
ENST00000414786.7:n.3627G>C
ENST00000445220.7:c.2095G>C ENSP00000489407.2:p.Ala699Pro
ENST00000664402.2:c.1585G>C ENSP00000499475.1:p.Ala529Pro
ENST00000673971.2:c.*2041G>C ENSP00000501192.1:n.*2041G>C
ENST00000445220.6:c.2095G>C ENSP00000489407.2:p.Ala699Pro
ENST00000262795.6:c.3043G>C ENSP00000489147.2:p.Ala1015Pro
ENST00000664402.1:c.1585G>C ENSP00000499475.1:p.Ala529Pro
ENST00000673971.1:c.*2041G>C ENSP00000501192.1:n.*2041G>C
ENST00000262795.5:c.3439G>C ENSP00000489147.1:p.Ala1147Pro
ENST00000414786.6:n.3627G>C
ENST00000445220.5:c.3421G>C ENSP00000489407.1:p.Ala1141Pro