Canonical Allele Identifier: CA1981067957
Gene: SHANK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.70473229G= , CM000673.2:g.70473229G= GRCh38
NC_000011.9:g.70319334G= , CM000673.1:g.70319334G= GRCh37
NC_000011.8:g.69996982G= NCBI36
NG_042866.1:g.656568C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000338508.9:c.3423C= ENSP00000345193.7:p.Thr1141=
ENST00000412252.6:c.968C= ENSP00000414876.2:n.968C=
ENST00000601538.6:c.5190C= MANE Select ENSP00000469689.2:p.Thr1730=
ENST00000654939.1:c.2699C=
ENST00000656230.1:c.4053C= ENSP00000499561.1:p.Thr1351=
ENST00000659264.1:c.3480C= ENSP00000499270.1:p.Thr1160=
ENST00000338508.8:c.3426C= ENSP00000345193.6:p.Thr1142=
ENST00000357171.7:c.*194C= ENSP00000349694.4:n.*194C=
ENST00000409161.5:c.3402C= ENSP00000386491.1:p.Thr1134=
ENST00000412252.5:c.966C=
ENST00000423696.6:c.4053C= ENSP00000394536.2:p.Thr1351=
ENST00000424924.5:c.3027C= ENSP00000402944.1:p.Thr1009=
ENST00000449833.6:c.3426C= ENSP00000399423.3:p.Thr1142=
ENST00000601538.5:c.5190C= ENSP00000469689.2:p.Thr1730=
ENST00000606715.3:n.1942C=
NM_012309.4:c.5190C= NP_036441.2:p.Thr1730=
NM_133266.4:c.3426C= NP_573573.2:p.Thr1142=
NR_110766.1:n.1044C=
XM_005277930.2:c.5190C= XP_005277987.1:p.Thr1730=
XM_005277932.2:c.4053C= XP_005277989.1:p.Thr1351=
XM_006718478.2:c.5160C= XP_006718541.1:p.Thr1720=
XM_011544854.1:c.5202C= XP_011543156.1:p.Thr1734=
XM_011544855.1:c.5181C= XP_011543157.1:p.Thr1727=
XM_011544856.1:c.5175C= XP_011543158.1:p.Thr1725=
XM_011544857.1:c.5154C= XP_011543159.1:p.Thr1718=
XM_011544859.1:c.4065C= XP_011543161.1:p.Thr1355=
XM_005277932.3:c.4053C= XP_005277989.1:p.Thr1351=
XM_017017387.1:c.5190C= XP_016872876.1:p.Thr1730=
XM_017017388.1:c.5190C= XP_016872877.1:p.Thr1730=
XM_017017389.1:c.5163C= XP_016872878.1:p.Thr1721=
XM_017017390.1:c.3480C= XP_016872879.1:p.Thr1160=
NM_133266.5:c.3426C= NP_573573.2:p.Thr1142=
NR_110766.2:n.1045C=
NM_001379226.1:c.4053C= NP_001366155.1:p.Thr1351=
NM_012309.5:c.5190C= MANE Select NP_036441.2:p.Thr1730=