Canonical Allele Identifier: CA515259696
Gene: SHANK3 HGNC NCBI

Linked Data

dbSNP Id: rs922625356
MyVariant Identifiers: chr22:g.51159013C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50720585C>T , CM000684.2:g.50720585C>T GRCh38
NC_000022.10:g.51159013C>T , CM000684.1:g.51159013C>T GRCh37
NC_000022.9:g.49505879C>T NCBI36
NG_008607.2:g.51231C>T
NG_070230.1:g.56369C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.2353C>T ENSP00000489147.2:p.Pro785Ser
ENST00000414786.7:n.2937C>T
ENST00000445220.7:c.1405C>T ENSP00000489407.2:p.Pro469Ser
ENST00000664402.2:c.895C>T ENSP00000499475.1:p.Pro299Ser
ENST00000673971.2:c.*1351C>T ENSP00000501192.1:n.*1351C>T
ENST00000445220.6:c.1405C>T ENSP00000489407.2:p.Pro469Ser
ENST00000262795.6:c.2353C>T ENSP00000489147.2:p.Pro785Ser
ENST00000664402.1:c.895C>T ENSP00000499475.1:p.Pro299Ser
ENST00000673971.1:c.*1351C>T ENSP00000501192.1:n.*1351C>T
ENST00000262795.5:c.2749C>T ENSP00000489147.1:p.Pro917Ser
ENST00000414786.6:n.2937C>T
ENST00000445220.5:c.2731C>T ENSP00000489407.1:p.Pro911Ser