Canonical Allele Identifier: CA515259831
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51159060C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50720632C>A , CM000684.2:g.50720632C>A GRCh38
NC_000022.10:g.51159060C>A , CM000684.1:g.51159060C>A GRCh37
NC_000022.9:g.49505926C>A NCBI36
NG_008607.2:g.51278C>A
NG_070230.1:g.56416C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.2400C>A ENSP00000489147.2:p.Asn800Lys
ENST00000414786.7:n.2984C>A
ENST00000445220.7:c.1452C>A ENSP00000489407.2:p.Asn484Lys
ENST00000664402.2:c.942C>A ENSP00000499475.1:p.Asn314Lys
ENST00000673971.2:c.*1398C>A ENSP00000501192.1:n.*1398C>A
ENST00000445220.6:c.1452C>A ENSP00000489407.2:p.Asn484Lys
ENST00000262795.6:c.2400C>A ENSP00000489147.2:p.Asn800Lys
ENST00000664402.1:c.942C>A ENSP00000499475.1:p.Asn314Lys
ENST00000673971.1:c.*1398C>A ENSP00000501192.1:n.*1398C>A
ENST00000262795.5:c.2796C>A ENSP00000489147.1:p.Asn932Lys
ENST00000414786.6:n.2984C>A
ENST00000445220.5:c.2778C>A ENSP00000489407.1:p.Asn926Lys