Canonical Allele Identifier: CA515261334
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51159591T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50721163T>G , CM000684.2:g.50721163T>G GRCh38
NC_000022.10:g.51159591T>G , CM000684.1:g.51159591T>G GRCh37
NC_000022.9:g.49506457T>G NCBI36
NG_008607.2:g.51809T>G
NG_070230.1:g.56947T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.2931T>G ENSP00000489147.2:p.Leu977=
ENST00000414786.7:n.3515T>G
ENST00000445220.7:c.1983T>G ENSP00000489407.2:p.Leu661=
ENST00000664402.2:c.1473T>G ENSP00000499475.1:p.Leu491=
ENST00000673971.2:c.*1929T>G ENSP00000501192.1:n.*1929T>G
ENST00000445220.6:c.1983T>G ENSP00000489407.2:p.Leu661=
ENST00000262795.6:c.2931T>G ENSP00000489147.2:p.Leu977=
ENST00000664402.1:c.1473T>G ENSP00000499475.1:p.Leu491=
ENST00000673971.1:c.*1929T>G ENSP00000501192.1:n.*1929T>G
ENST00000262795.5:c.3327T>G ENSP00000489147.1:p.Leu1109=
ENST00000414786.6:n.3515T>G
ENST00000445220.5:c.3309T>G ENSP00000489407.1:p.Leu1103=