Canonical Allele Identifier: CA515264748
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51160630G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50722202G>A , CM000684.2:g.50722202G>A GRCh38
NC_000022.10:g.51160630G>A , CM000684.1:g.51160630G>A GRCh37
NC_000022.9:g.49507496G>A NCBI36
NG_008607.2:g.52848G>A
NG_070230.1:g.57986G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.3970G>A ENSP00000489147.2:p.Ala1324Thr
ENST00000414786.7:n.4554G>A
ENST00000445220.7:c.3022G>A ENSP00000489407.2:p.Ala1008Thr
ENST00000664402.2:c.2512G>A ENSP00000499475.1:p.Ala838Thr
ENST00000673971.2:c.*2968G>A ENSP00000501192.1:n.*2968G>A
ENST00000445220.6:c.3022G>A ENSP00000489407.2:p.Ala1008Thr
ENST00000262795.6:c.3970G>A ENSP00000489147.2:p.Ala1324Thr
ENST00000664402.1:c.2512G>A ENSP00000499475.1:p.Ala838Thr
ENST00000673971.1:c.*2968G>A ENSP00000501192.1:n.*2968G>A
ENST00000262795.5:c.4366G>A ENSP00000489147.1:p.Ala1456Thr
ENST00000414786.6:n.4554G>A
ENST00000445220.5:c.4348G>A ENSP00000489407.1:p.Ala1450Thr