Canonical Allele Identifier: CA515264772
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51160637G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50722209G>T , CM000684.2:g.50722209G>T GRCh38
NC_000022.10:g.51160637G>T , CM000684.1:g.51160637G>T GRCh37
NC_000022.9:g.49507503G>T NCBI36
NG_008607.2:g.52855G>T
NG_070230.1:g.57993G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.3977G>T ENSP00000489147.2:p.Gly1326Val
ENST00000414786.7:n.4561G>T
ENST00000445220.7:c.3029G>T ENSP00000489407.2:p.Gly1010Val
ENST00000664402.2:c.2519G>T ENSP00000499475.1:p.Gly840Val
ENST00000673971.2:c.*2975G>T ENSP00000501192.1:n.*2975G>T
ENST00000445220.6:c.3029G>T ENSP00000489407.2:p.Gly1010Val
ENST00000262795.6:c.3977G>T ENSP00000489147.2:p.Gly1326Val
ENST00000664402.1:c.2519G>T ENSP00000499475.1:p.Gly840Val
ENST00000673971.1:c.*2975G>T ENSP00000501192.1:n.*2975G>T
ENST00000262795.5:c.4373G>T ENSP00000489147.1:p.Gly1458Val
ENST00000414786.6:n.4561G>T
ENST00000445220.5:c.4355G>T ENSP00000489407.1:p.Gly1452Val