Canonical Allele Identifier: CA515264174
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51160435C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50722007C>G , CM000684.2:g.50722007C>G GRCh38
NC_000022.10:g.51160435C>G , CM000684.1:g.51160435C>G GRCh37
NC_000022.9:g.49507301C>G NCBI36
NG_008607.2:g.52653C>G
NG_070230.1:g.57791C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.3775C>G ENSP00000489147.2:p.Leu1259Val
ENST00000414786.7:n.4359C>G
ENST00000445220.7:c.2827C>G ENSP00000489407.2:p.Leu943Val
ENST00000664402.2:c.2317C>G ENSP00000499475.1:p.Leu773Val
ENST00000673971.2:c.*2773C>G ENSP00000501192.1:n.*2773C>G
ENST00000445220.6:c.2827C>G ENSP00000489407.2:p.Leu943Val
ENST00000262795.6:c.3775C>G ENSP00000489147.2:p.Leu1259Val
ENST00000664402.1:c.2317C>G ENSP00000499475.1:p.Leu773Val
ENST00000673971.1:c.*2773C>G ENSP00000501192.1:n.*2773C>G
ENST00000262795.5:c.4171C>G ENSP00000489147.1:p.Leu1391Val
ENST00000414786.6:n.4359C>G
ENST00000445220.5:c.4153C>G ENSP00000489407.1:p.Leu1385Val