Canonical Allele Identifier: CA515263376
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51160177T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50721749T>A , CM000684.2:g.50721749T>A GRCh38
NC_000022.10:g.51160177T>A , CM000684.1:g.51160177T>A GRCh37
NC_000022.9:g.49507043T>A NCBI36
NG_008607.2:g.52395T>A
NG_070230.1:g.57533T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.3517T>A ENSP00000489147.2:p.Leu1173Met
ENST00000414786.7:n.4101T>A
ENST00000445220.7:c.2569T>A ENSP00000489407.2:p.Leu857Met
ENST00000664402.2:c.2059T>A ENSP00000499475.1:p.Leu687Met
ENST00000673971.2:c.*2515T>A ENSP00000501192.1:n.*2515T>A
ENST00000445220.6:c.2569T>A ENSP00000489407.2:p.Leu857Met
ENST00000262795.6:c.3517T>A ENSP00000489147.2:p.Leu1173Met
ENST00000664402.1:c.2059T>A ENSP00000499475.1:p.Leu687Met
ENST00000673971.1:c.*2515T>A ENSP00000501192.1:n.*2515T>A
ENST00000262795.5:c.3913T>A ENSP00000489147.1:p.Leu1305Met
ENST00000414786.6:n.4101T>A
ENST00000445220.5:c.3895T>A ENSP00000489407.1:p.Leu1299Met