Canonical Allele Identifier: CA515262231
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51159815G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50721387G>T , CM000684.2:g.50721387G>T GRCh38
NC_000022.10:g.51159815G>T , CM000684.1:g.51159815G>T GRCh37
NC_000022.9:g.49506681G>T NCBI36
NG_008607.2:g.52033G>T
NG_070230.1:g.57171G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.3155G>T ENSP00000489147.2:p.Arg1052Leu
ENST00000414786.7:n.3739G>T
ENST00000445220.7:c.2207G>T ENSP00000489407.2:p.Arg736Leu
ENST00000664402.2:c.1697G>T ENSP00000499475.1:p.Arg566Leu
ENST00000673971.2:c.*2153G>T ENSP00000501192.1:n.*2153G>T
ENST00000445220.6:c.2207G>T ENSP00000489407.2:p.Arg736Leu
ENST00000262795.6:c.3155G>T ENSP00000489147.2:p.Arg1052Leu
ENST00000664402.1:c.1697G>T ENSP00000499475.1:p.Arg566Leu
ENST00000673971.1:c.*2153G>T ENSP00000501192.1:n.*2153G>T
ENST00000262795.5:c.3551G>T ENSP00000489147.1:p.Arg1184Leu
ENST00000414786.6:n.3739G>T
ENST00000445220.5:c.3533G>T ENSP00000489407.1:p.Arg1178Leu