Canonical Allele Identifier: CA515261708
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51159723G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50721295G>T , CM000684.2:g.50721295G>T GRCh38
NC_000022.10:g.51159723G>T , CM000684.1:g.51159723G>T GRCh37
NC_000022.9:g.49506589G>T NCBI36
NG_008607.2:g.51941G>T
NG_070230.1:g.57079G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.3063G>T ENSP00000489147.2:p.Gly1021=
ENST00000414786.7:n.3647G>T
ENST00000445220.7:c.2115G>T ENSP00000489407.2:p.Gly705=
ENST00000664402.2:c.1605G>T ENSP00000499475.1:p.Gly535=
ENST00000673971.2:c.*2061G>T ENSP00000501192.1:n.*2061G>T
ENST00000445220.6:c.2115G>T ENSP00000489407.2:p.Gly705=
ENST00000262795.6:c.3063G>T ENSP00000489147.2:p.Gly1021=
ENST00000664402.1:c.1605G>T ENSP00000499475.1:p.Gly535=
ENST00000673971.1:c.*2061G>T ENSP00000501192.1:n.*2061G>T
ENST00000262795.5:c.3459G>T ENSP00000489147.1:p.Gly1153=
ENST00000414786.6:n.3647G>T
ENST00000445220.5:c.3441G>T ENSP00000489407.1:p.Gly1147=