Canonical Allele Identifier: CA515259819

Gene: SHANK3

Linked Data

• gnomAD v4: 22-50720628-C-A
• MyVariant Identifiers: chr22:g.51159056C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50720628C>A , CM000684.2:g.50720628C>A	GRCh38
NC_000022.10:g.51159056C>A , CM000684.1:g.51159056C>A	GRCh37
NC_000022.9:g.49505922C>A	NCBI36
NG_008607.2:g.51274C>A
NG_070230.1:g.56412C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262795.7:c.2396C>A	ENSP00000489147.2:p.Ala799Asp
ENST00000414786.7:n.2980C>A
ENST00000445220.7:c.1448C>A	ENSP00000489407.2:p.Ala483Asp
ENST00000664402.2:c.938C>A	ENSP00000499475.1:p.Ala313Asp
ENST00000673971.2:c.*1394C>A	ENSP00000501192.1:n.*1394C>A
ENST00000445220.6:c.1448C>A	ENSP00000489407.2:p.Ala483Asp
ENST00000262795.6:c.2396C>A	ENSP00000489147.2:p.Ala799Asp
ENST00000664402.1:c.938C>A	ENSP00000499475.1:p.Ala313Asp
ENST00000673971.1:c.*1394C>A	ENSP00000501192.1:n.*1394C>A
ENST00000262795.5:c.2792C>A	ENSP00000489147.1:p.Ala931Asp
ENST00000414786.6:n.2980C>A
ENST00000445220.5:c.2774C>A	ENSP00000489407.1:p.Ala925Asp