Canonical Allele Identifier: CA515263406

Gene: SHANK3

Linked Data

• dbSNP Id: rs1184106700
• gnomAD v2: 22-51160187-C-T
• gnomAD v4: 22-50721759-C-T
• MyVariant Identifiers: chr22:g.51160187C>T (hg19) ; chr22:g.50721759C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50721759C>T , CM000684.2:g.50721759C>T	GRCh38
NC_000022.10:g.51160187C>T , CM000684.1:g.51160187C>T	GRCh37
NC_000022.9:g.49507053C>T	NCBI36
NG_008607.2:g.52405C>T
NG_070230.1:g.57543C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262795.7:c.3527C>T	ENSP00000489147.2:p.Pro1176Leu
ENST00000414786.7:n.4111C>T
ENST00000445220.7:c.2579C>T	ENSP00000489407.2:p.Pro860Leu
ENST00000664402.2:c.2069C>T	ENSP00000499475.1:p.Pro690Leu
ENST00000673971.2:c.*2525C>T	ENSP00000501192.1:n.*2525C>T
ENST00000445220.6:c.2579C>T	ENSP00000489407.2:p.Pro860Leu
ENST00000262795.6:c.3527C>T	ENSP00000489147.2:p.Pro1176Leu
ENST00000664402.1:c.2069C>T	ENSP00000499475.1:p.Pro690Leu
ENST00000673971.1:c.*2525C>T	ENSP00000501192.1:n.*2525C>T
ENST00000262795.5:c.3923C>T	ENSP00000489147.1:p.Pro1308Leu
ENST00000414786.6:n.4111C>T
ENST00000445220.5:c.3905C>T	ENSP00000489407.1:p.Pro1302Leu