Canonical Allele Identifier: CA10325960

Gene: SHANK3

Linked Data

• dbSNP Id: rs774184196
• ExAC: 22:51159384 C / T
• gnomAD v2: 22-51159384-C-T
• gnomAD v3: 22-50720956-C-T
• gnomAD v4: 22-50720956-C-T
• MyVariant Identifiers: chr22:g.51159384C>T (hg19) ; chr22:g.50720956C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50720956C>T , CM000684.2:g.50720956C>T	GRCh38
NC_000022.10:g.51159384C>T , CM000684.1:g.51159384C>T	GRCh37
NC_000022.9:g.49506250C>T	NCBI36
NG_008607.2:g.51602C>T
NG_070230.1:g.56740C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262795.7:c.2724C>T	ENSP00000489147.2:p.Gly908=
ENST00000414786.7:n.3308C>T
ENST00000445220.7:c.1776C>T	ENSP00000489407.2:p.Gly592=
ENST00000664402.2:c.1266C>T	ENSP00000499475.1:p.Gly422=
ENST00000673971.2:c.*1722C>T	ENSP00000501192.1:n.*1722C>T
ENST00000445220.6:c.1776C>T	ENSP00000489407.2:p.Gly592=
ENST00000262795.6:c.2724C>T	ENSP00000489147.2:p.Gly908=
ENST00000664402.1:c.1266C>T	ENSP00000499475.1:p.Gly422=
ENST00000673971.1:c.*1722C>T	ENSP00000501192.1:n.*1722C>T
ENST00000262795.5:c.3120C>T	ENSP00000489147.1:p.Gly1040=
ENST00000414786.6:n.3308C>T
ENST00000445220.5:c.3102C>T	ENSP00000489407.1:p.Gly1034=