Canonical Allele Identifier: CA1981067931

Gene: SHANK2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.70473161A= , CM000673.2:g.70473161A=	GRCh38
NC_000011.9:g.70319266A= , CM000673.1:g.70319266A=	GRCh37
NC_000011.8:g.69996914A=	NCBI36
NG_042866.1:g.656636T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338508.9:c.3491T=	ENSP00000345193.7:p.Phe1164=
ENST00000412252.6:c.1036T=	ENSP00000414876.2:n.1036T=
ENST00000601538.6:c.5258T= MANE Select	ENSP00000469689.2:p.Phe1753=
ENST00000654939.1:c.2767T=
ENST00000656230.1:c.4121T=	ENSP00000499561.1:p.Phe1374=
ENST00000659264.1:c.3548T=	ENSP00000499270.1:p.Phe1183=
ENST00000338508.8:c.3494T=	ENSP00000345193.6:p.Phe1165=
ENST00000357171.7:c.*262T=	ENSP00000349694.4:n.*262T=
ENST00000409161.5:c.3470T=	ENSP00000386491.1:p.Phe1157=
ENST00000412252.5:c.1034T=
ENST00000423696.6:c.4121T=	ENSP00000394536.2:p.Phe1374=
ENST00000424924.5:c.3095T=	ENSP00000402944.1:p.Phe1032=
ENST00000449833.6:c.3494T=	ENSP00000399423.3:p.Phe1165=
ENST00000601538.5:c.5258T=	ENSP00000469689.2:p.Phe1753=
ENST00000606715.3:n.2010T=
NM_012309.4:c.5258T=	NP_036441.2:p.Phe1753=
NM_133266.4:c.3494T=	NP_573573.2:p.Phe1165=
NR_110766.1:n.1112T=
XM_005277930.2:c.5258T=	XP_005277987.1:p.Phe1753=
XM_005277932.2:c.4121T=	XP_005277989.1:p.Phe1374=
XM_006718478.2:c.5228T=	XP_006718541.1:p.Phe1743=
XM_011544854.1:c.5270T=	XP_011543156.1:p.Phe1757=
XM_011544855.1:c.5249T=	XP_011543157.1:p.Phe1750=
XM_011544856.1:c.5243T=	XP_011543158.1:p.Phe1748=
XM_011544857.1:c.5222T=	XP_011543159.1:p.Phe1741=
XM_011544859.1:c.4133T=	XP_011543161.1:p.Phe1378=
XM_005277932.3:c.4121T=	XP_005277989.1:p.Phe1374=
XM_017017387.1:c.5258T=	XP_016872876.1:p.Phe1753=
XM_017017388.1:c.5258T=	XP_016872877.1:p.Phe1753=
XM_017017389.1:c.5231T=	XP_016872878.1:p.Phe1744=
XM_017017390.1:c.3548T=	XP_016872879.1:p.Phe1183=
NM_133266.5:c.3494T=	NP_573573.2:p.Phe1165=
NR_110766.2:n.1113T=
NM_001379226.1:c.4121T=	NP_001366155.1:p.Phe1374=
NM_012309.5:c.5258T= MANE Select	NP_036441.2:p.Phe1753=