Canonical Allele Identifier: CA10326090

Gene: SHANK3

Linked Data

• dbSNP Id: rs764950597
• ExAC: 22:51159900 C / T
• gnomAD v2: 22-51159900-C-T
• gnomAD v3: 22-50721472-C-T
• gnomAD v4: 22-50721472-C-T
• MyVariant Identifiers: chr22:g.51159900C>T (hg19) ; chr22:g.50721472C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50721472C>T , CM000684.2:g.50721472C>T	GRCh38
NC_000022.10:g.51159900C>T , CM000684.1:g.51159900C>T	GRCh37
NC_000022.9:g.49506766C>T	NCBI36
NG_008607.2:g.52118C>T
NG_070230.1:g.57256C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262795.7:c.3240C>T	ENSP00000489147.2:p.His1080=
ENST00000414786.7:n.3824C>T
ENST00000445220.7:c.2292C>T	ENSP00000489407.2:p.His764=
ENST00000664402.2:c.1782C>T	ENSP00000499475.1:p.His594=
ENST00000673971.2:c.*2238C>T	ENSP00000501192.1:n.*2238C>T
ENST00000445220.6:c.2292C>T	ENSP00000489407.2:p.His764=
ENST00000262795.6:c.3240C>T	ENSP00000489147.2:p.His1080=
ENST00000664402.1:c.1782C>T	ENSP00000499475.1:p.His594=
ENST00000673971.1:c.*2238C>T	ENSP00000501192.1:n.*2238C>T
ENST00000262795.5:c.3636C>T	ENSP00000489147.1:p.His1212=
ENST00000414786.6:n.3824C>T
ENST00000445220.5:c.3618C>T	ENSP00000489407.1:p.His1206=