Canonical Allele Identifier: CA515262108
Gene: SHANK3 HGNC NCBI

Linked Data

dbSNP Id: rs2083286192
MyVariant Identifiers: chr22:g.51159779C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50721351C>A , CM000684.2:g.50721351C>A GRCh38
NC_000022.10:g.51159779C>A , CM000684.1:g.51159779C>A GRCh37
NC_000022.9:g.49506645C>A NCBI36
NG_008607.2:g.51997C>A
NG_070230.1:g.57135C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.3119C>A ENSP00000489147.2:p.Ala1040Asp
ENST00000414786.7:n.3703C>A
ENST00000445220.7:c.2171C>A ENSP00000489407.2:p.Ala724Asp
ENST00000664402.2:c.1661C>A ENSP00000499475.1:p.Ala554Asp
ENST00000673971.2:c.*2117C>A ENSP00000501192.1:n.*2117C>A
ENST00000445220.6:c.2171C>A ENSP00000489407.2:p.Ala724Asp
ENST00000262795.6:c.3119C>A ENSP00000489147.2:p.Ala1040Asp
ENST00000664402.1:c.1661C>A ENSP00000499475.1:p.Ala554Asp
ENST00000673971.1:c.*2117C>A ENSP00000501192.1:n.*2117C>A
ENST00000262795.5:c.3515C>A ENSP00000489147.1:p.Ala1172Asp
ENST00000414786.6:n.3703C>A
ENST00000445220.5:c.3497C>A ENSP00000489407.1:p.Ala1166Asp