Canonical Allele Identifier: CA515254922
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51136020C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50697592C>A , CM000684.2:g.50697592C>A GRCh38
NC_000022.10:g.51136020C>A , CM000684.1:g.51136020C>A GRCh37
NC_000022.9:g.49482886C>A NCBI36
NG_008607.2:g.28238C>A
NG_070230.1:g.33457C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000262795.7:c.976C>A ENSP00000489147.2:p.Pro326Thr
ENST00000414786.7:n.1560C>A
ENST00000445220.7:c.28C>A ENSP00000489407.2:p.Pro10Thr
ENST00000673971.2:c.1333C>A ENSP00000501192.1:p.Pro445Thr
ENST00000445220.6:c.28C>A ENSP00000489407.2:p.Pro10Thr
ENST00000262795.6:c.976C>A ENSP00000489147.2:p.Pro326Thr
ENST00000673971.1:c.1333C>A ENSP00000501192.1:p.Pro445Thr
ENST00000673995.1:c.29C>A
ENST00000262795.5:c.1372C>A ENSP00000489147.1:p.Pro458Thr
ENST00000414786.6:n.1560C>A
ENST00000445220.5:c.1354C>A ENSP00000489407.1:p.Pro452Thr