Canonical Allele Identifier: CA1981345980

Gene: SHANK2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.71147071C= , CM000673.2:g.71147071C=	GRCh38
NC_000011.9:g.70858117C= , CM000673.1:g.70858117C=	GRCh37
NC_000011.8:g.70535765C=	NCBI36
NG_042866.1:g.82726G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000601538.6:c.207+49G= MANE Select	ENSP00000469689.2:n.207+49G=
ENST00000601538.5:c.207+49G=	ENSP00000469689.2:n.207+49G=
ENST00000608988.5:c.207+49G=	ENSP00000476264.2:n.207+49G=
NM_012309.4:c.207+49G=	NP_036441.2:n.207+49G=
XM_005277930.2:c.207+49G=	XP_005277987.1:n.207+49G=
XM_006718478.2:c.207+49G=	XP_006718541.1:n.207+49G=
XM_011544854.1:c.207+49G=	XP_011543156.1:n.207+49G=
XM_011544855.1:c.207+49G=	XP_011543157.1:n.207+49G=
XM_011544856.1:c.207+49G=	XP_011543158.1:n.207+49G=
XM_011544857.1:c.207+49G=	XP_011543159.1:n.207+49G=
XM_011544858.1:c.207+49G=	XP_011543160.1:n.207+49G=
XM_017017387.1:c.207+49G=	XP_016872876.1:n.207+49G=
XM_017017388.1:c.207+49G=	XP_016872877.1:n.207+49G=
XM_017017389.1:c.207+49G=	XP_016872878.1:n.207+49G=
NM_012309.5:c.207+49G= MANE Select	NP_036441.2:n.207+49G=