Canonical Allele Identifier: CA515262073
Gene: SHANK3 HGNC NCBI

Linked Data

dbSNP Id: rs2083286037
MyVariant Identifiers: chr22:g.51159768T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50721340T>G , CM000684.2:g.50721340T>G GRCh38
NC_000022.10:g.51159768T>G , CM000684.1:g.51159768T>G GRCh37
NC_000022.9:g.49506634T>G NCBI36
NG_008607.2:g.51986T>G
NG_070230.1:g.57124T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.3108T>G ENSP00000489147.2:p.Ile1036Met
ENST00000414786.7:n.3692T>G
ENST00000445220.7:c.2160T>G ENSP00000489407.2:p.Ile720Met
ENST00000664402.2:c.1650T>G ENSP00000499475.1:p.Ile550Met
ENST00000673971.2:c.*2106T>G ENSP00000501192.1:n.*2106T>G
ENST00000445220.6:c.2160T>G ENSP00000489407.2:p.Ile720Met
ENST00000262795.6:c.3108T>G ENSP00000489147.2:p.Ile1036Met
ENST00000664402.1:c.1650T>G ENSP00000499475.1:p.Ile550Met
ENST00000673971.1:c.*2106T>G ENSP00000501192.1:n.*2106T>G
ENST00000262795.5:c.3504T>G ENSP00000489147.1:p.Ile1168Met
ENST00000414786.6:n.3692T>G
ENST00000445220.5:c.3486T>G ENSP00000489407.1:p.Ile1162Met