Canonical Allele Identifier: CA381675754
Gene: SHANK2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.70473132A>G , CM000673.2:g.70473132A>G GRCh38
NC_000011.9:g.70319237A>G , CM000673.1:g.70319237A>G GRCh37
NC_000011.8:g.69996885A>G NCBI36
NG_042866.1:g.656665T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000338508.9:c.3520T>C ENSP00000345193.7:p.Ser1174Pro
ENST00000412252.6:c.1065T>C ENSP00000414876.2:n.1065T>C
ENST00000601538.6:c.5287T>C MANE Select ENSP00000469689.2:p.Ser1763Pro
ENST00000654939.1:c.2796T>C
ENST00000656230.1:c.4150T>C ENSP00000499561.1:p.Ser1384Pro
ENST00000659264.1:c.3577T>C ENSP00000499270.1:p.Ser1193Pro
ENST00000338508.8:c.3523T>C ENSP00000345193.6:p.Ser1175Pro
ENST00000357171.7:c.*291T>C ENSP00000349694.4:n.*291T>C
ENST00000409161.5:c.3499T>C ENSP00000386491.1:p.Ser1167Pro
ENST00000412252.5:c.1063T>C
ENST00000423696.6:c.4150T>C ENSP00000394536.2:p.Ser1384Pro
ENST00000424924.5:c.3124T>C ENSP00000402944.1:p.Ser1042Pro
ENST00000449833.6:c.3523T>C ENSP00000399423.3:p.Ser1175Pro
ENST00000601538.5:c.5287T>C ENSP00000469689.2:p.Ser1763Pro
ENST00000606715.3:n.2039T>C
NM_012309.4:c.5287T>C NP_036441.2:p.Ser1763Pro
NM_133266.4:c.3523T>C NP_573573.2:p.Ser1175Pro
NR_110766.1:n.1141T>C
XM_005277930.2:c.5287T>C XP_005277987.1:p.Ser1763Pro
XM_005277932.2:c.4150T>C XP_005277989.1:p.Ser1384Pro
XM_006718478.2:c.5257T>C XP_006718541.1:p.Ser1753Pro
XM_011544854.1:c.5299T>C XP_011543156.1:p.Ser1767Pro
XM_011544855.1:c.5278T>C XP_011543157.1:p.Ser1760Pro
XM_011544856.1:c.5272T>C XP_011543158.1:p.Ser1758Pro
XM_011544857.1:c.5251T>C XP_011543159.1:p.Ser1751Pro
XM_011544859.1:c.4162T>C XP_011543161.1:p.Ser1388Pro
XM_005277932.3:c.4150T>C XP_005277989.1:p.Ser1384Pro
XM_017017387.1:c.5287T>C XP_016872876.1:p.Ser1763Pro
XM_017017388.1:c.5287T>C XP_016872877.1:p.Ser1763Pro
XM_017017389.1:c.5260T>C XP_016872878.1:p.Ser1754Pro
XM_017017390.1:c.3577T>C XP_016872879.1:p.Ser1193Pro
NM_133266.5:c.3523T>C NP_573573.2:p.Ser1175Pro
NR_110766.2:n.1142T>C
NM_001379226.1:c.4150T>C NP_001366155.1:p.Ser1384Pro
NM_012309.5:c.5287T>C MANE Select NP_036441.2:p.Ser1763Pro