Canonical Allele Identifier: CA515261311
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51159584T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50721156T>G , CM000684.2:g.50721156T>G GRCh38
NC_000022.10:g.51159584T>G , CM000684.1:g.51159584T>G GRCh37
NC_000022.9:g.49506450T>G NCBI36
NG_008607.2:g.51802T>G
NG_070230.1:g.56940T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.2924T>G ENSP00000489147.2:p.Leu975Arg
ENST00000414786.7:n.3508T>G
ENST00000445220.7:c.1976T>G ENSP00000489407.2:p.Leu659Arg
ENST00000664402.2:c.1466T>G ENSP00000499475.1:p.Leu489Arg
ENST00000673971.2:c.*1922T>G ENSP00000501192.1:n.*1922T>G
ENST00000445220.6:c.1976T>G ENSP00000489407.2:p.Leu659Arg
ENST00000262795.6:c.2924T>G ENSP00000489147.2:p.Leu975Arg
ENST00000664402.1:c.1466T>G ENSP00000499475.1:p.Leu489Arg
ENST00000673971.1:c.*1922T>G ENSP00000501192.1:n.*1922T>G
ENST00000262795.5:c.3320T>G ENSP00000489147.1:p.Leu1107Arg
ENST00000414786.6:n.3508T>G
ENST00000445220.5:c.3302T>G ENSP00000489407.1:p.Leu1101Arg