Canonical Allele Identifier: CA515264779
Gene: SHANK3 HGNC NCBI

Linked Data

dbSNP Id: rs2083297666
MyVariant Identifiers: chr22:g.51160639C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50722211C>T , CM000684.2:g.50722211C>T GRCh38
NC_000022.10:g.51160639C>T , CM000684.1:g.51160639C>T GRCh37
NC_000022.9:g.49507505C>T NCBI36
NG_008607.2:g.52857C>T
NG_070230.1:g.57995C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.3979C>T ENSP00000489147.2:p.Pro1327Ser
ENST00000414786.7:n.4563C>T
ENST00000445220.7:c.3031C>T ENSP00000489407.2:p.Pro1011Ser
ENST00000664402.2:c.2521C>T ENSP00000499475.1:p.Pro841Ser
ENST00000673971.2:c.*2977C>T ENSP00000501192.1:n.*2977C>T
ENST00000445220.6:c.3031C>T ENSP00000489407.2:p.Pro1011Ser
ENST00000262795.6:c.3979C>T ENSP00000489147.2:p.Pro1327Ser
ENST00000664402.1:c.2521C>T ENSP00000499475.1:p.Pro841Ser
ENST00000673971.1:c.*2977C>T ENSP00000501192.1:n.*2977C>T
ENST00000262795.5:c.4375C>T ENSP00000489147.1:p.Pro1459Ser
ENST00000414786.6:n.4563C>T
ENST00000445220.5:c.4357C>T ENSP00000489407.1:p.Pro1453Ser