Canonical Allele Identifier: CA515261134
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51159520G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50721092G>T , CM000684.2:g.50721092G>T GRCh38
NC_000022.10:g.51159520G>T , CM000684.1:g.51159520G>T GRCh37
NC_000022.9:g.49506386G>T NCBI36
NG_008607.2:g.51738G>T
NG_070230.1:g.56876G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.2860G>T ENSP00000489147.2:p.Gly954Trp
ENST00000414786.7:n.3444G>T
ENST00000445220.7:c.1912G>T ENSP00000489407.2:p.Gly638Trp
ENST00000664402.2:c.1402G>T ENSP00000499475.1:p.Gly468Trp
ENST00000673971.2:c.*1858G>T ENSP00000501192.1:n.*1858G>T
ENST00000445220.6:c.1912G>T ENSP00000489407.2:p.Gly638Trp
ENST00000262795.6:c.2860G>T ENSP00000489147.2:p.Gly954Trp
ENST00000664402.1:c.1402G>T ENSP00000499475.1:p.Gly468Trp
ENST00000673971.1:c.*1858G>T ENSP00000501192.1:n.*1858G>T
ENST00000262795.5:c.3256G>T ENSP00000489147.1:p.Gly1086Trp
ENST00000414786.6:n.3444G>T
ENST00000445220.5:c.3238G>T ENSP00000489407.1:p.Gly1080Trp