Canonical Allele Identifier: CA515254947
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51136028G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50697600G>T , CM000684.2:g.50697600G>T GRCh38
NC_000022.10:g.51136028G>T , CM000684.1:g.51136028G>T GRCh37
NC_000022.9:g.49482894G>T NCBI36
NG_008607.2:g.28246G>T
NG_070230.1:g.33465G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.984G>T ENSP00000489147.2:p.Arg328=
ENST00000414786.7:n.1568G>T
ENST00000445220.7:c.36G>T ENSP00000489407.2:p.Arg12=
ENST00000673971.2:c.1341G>T ENSP00000501192.1:p.Arg447=
ENST00000445220.6:c.36G>T ENSP00000489407.2:p.Arg12=
ENST00000262795.6:c.984G>T ENSP00000489147.2:p.Arg328=
ENST00000673971.1:c.1341G>T ENSP00000501192.1:p.Arg447=
ENST00000673995.1:c.37G>T
ENST00000262795.5:c.1380G>T ENSP00000489147.1:p.Arg460=
ENST00000414786.6:n.1568G>T
ENST00000445220.5:c.1362G>T ENSP00000489407.1:p.Arg454=