Canonical Allele Identifier: CA515254868
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51136001C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50697573C>T , CM000684.2:g.50697573C>T GRCh38
NC_000022.10:g.51136001C>T , CM000684.1:g.51136001C>T GRCh37
NC_000022.9:g.49482867C>T NCBI36
NG_008607.2:g.28219C>T
NG_070230.1:g.33438C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.957C>T ENSP00000489147.2:p.Pro319=
ENST00000414786.7:n.1541C>T
ENST00000445220.7:c.9C>T ENSP00000489407.2:p.Pro3=
ENST00000673971.2:c.1314C>T ENSP00000501192.1:p.Pro438=
ENST00000445220.6:c.9C>T ENSP00000489407.2:p.Pro3=
ENST00000262795.6:c.957C>T ENSP00000489147.2:p.Pro319=
ENST00000673971.1:c.1314C>T ENSP00000501192.1:p.Pro438=
ENST00000673995.1:c.10C>T
ENST00000262795.5:c.1353C>T ENSP00000489147.1:p.Pro451=
ENST00000414786.6:n.1541C>T
ENST00000445220.5:c.1335C>T ENSP00000489407.1:p.Pro445=