Canonical Allele Identifier: CA515261403
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51159617T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50721189T>G , CM000684.2:g.50721189T>G GRCh38
NC_000022.10:g.51159617T>G , CM000684.1:g.51159617T>G GRCh37
NC_000022.9:g.49506483T>G NCBI36
NG_008607.2:g.51835T>G
NG_070230.1:g.56973T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.2957T>G ENSP00000489147.2:p.Leu986Arg
ENST00000414786.7:n.3541T>G
ENST00000445220.7:c.2009T>G ENSP00000489407.2:p.Leu670Arg
ENST00000664402.2:c.1499T>G ENSP00000499475.1:p.Leu500Arg
ENST00000673971.2:c.*1955T>G ENSP00000501192.1:n.*1955T>G
ENST00000445220.6:c.2009T>G ENSP00000489407.2:p.Leu670Arg
ENST00000262795.6:c.2957T>G ENSP00000489147.2:p.Leu986Arg
ENST00000664402.1:c.1499T>G ENSP00000499475.1:p.Leu500Arg
ENST00000673971.1:c.*1955T>G ENSP00000501192.1:n.*1955T>G
ENST00000262795.5:c.3353T>G ENSP00000489147.1:p.Leu1118Arg
ENST00000414786.6:n.3541T>G
ENST00000445220.5:c.3335T>G ENSP00000489407.1:p.Leu1112Arg