Canonical Allele Identifier: CA515261112

Gene: SHANK3

Linked Data

• dbSNP Id: rs1243460635
• gnomAD v2: 22-51159512-C-A
• gnomAD v4: 22-50721084-C-A
• MyVariant Identifiers: chr22:g.51159512C>A (hg19) ; chr22:g.50721084C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50721084C>A , CM000684.2:g.50721084C>A	GRCh38
NC_000022.10:g.51159512C>A , CM000684.1:g.51159512C>A	GRCh37
NC_000022.9:g.49506378C>A	NCBI36
NG_008607.2:g.51730C>A
NG_070230.1:g.56868C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262795.7:c.2852C>A	ENSP00000489147.2:p.Pro951Gln
ENST00000414786.7:n.3436C>A
ENST00000445220.7:c.1904C>A	ENSP00000489407.2:p.Pro635Gln
ENST00000664402.2:c.1394C>A	ENSP00000499475.1:p.Pro465Gln
ENST00000673971.2:c.*1850C>A	ENSP00000501192.1:n.*1850C>A
ENST00000445220.6:c.1904C>A	ENSP00000489407.2:p.Pro635Gln
ENST00000262795.6:c.2852C>A	ENSP00000489147.2:p.Pro951Gln
ENST00000664402.1:c.1394C>A	ENSP00000499475.1:p.Pro465Gln
ENST00000673971.1:c.*1850C>A	ENSP00000501192.1:n.*1850C>A
ENST00000262795.5:c.3248C>A	ENSP00000489147.1:p.Pro1083Gln
ENST00000414786.6:n.3436C>A
ENST00000445220.5:c.3230C>A	ENSP00000489407.1:p.Pro1077Gln