Canonical Allele Identifier: CA1981067906

Gene: SHANK2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.70473093T= , CM000673.2:g.70473093T=	GRCh38
NC_000011.9:g.70319198T= , CM000673.1:g.70319198T=	GRCh37
NC_000011.8:g.69996846T=	NCBI36
NG_042866.1:g.656704A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338508.9:c.3559A=	ENSP00000345193.7:p.Lys1187=
ENST00000412252.6:c.1104A=	ENSP00000414876.2:n.1104A=
ENST00000601538.6:c.5326A= MANE Select	ENSP00000469689.2:p.Lys1776=
ENST00000654939.1:c.2835A=
ENST00000656230.1:c.4189A=	ENSP00000499561.1:p.Lys1397=
ENST00000659264.1:c.3616A=	ENSP00000499270.1:p.Lys1206=
ENST00000338508.8:c.3562A=	ENSP00000345193.6:p.Lys1188=
ENST00000357171.7:c.*330A=	ENSP00000349694.4:n.*330A=
ENST00000409161.5:c.3538A=	ENSP00000386491.1:p.Lys1180=
ENST00000412252.5:c.1102A=
ENST00000423696.6:c.4189A=	ENSP00000394536.2:p.Lys1397=
ENST00000424924.5:c.3163A=	ENSP00000402944.1:p.Lys1055=
ENST00000449833.6:c.3562A=	ENSP00000399423.3:p.Lys1188=
ENST00000601538.5:c.5326A=	ENSP00000469689.2:p.Lys1776=
ENST00000606715.3:n.2078A=
NM_012309.4:c.5326A=	NP_036441.2:p.Lys1776=
NM_133266.4:c.3562A=	NP_573573.2:p.Lys1188=
NR_110766.1:n.1180A=
XM_005277930.2:c.5326A=	XP_005277987.1:p.Lys1776=
XM_005277932.2:c.4189A=	XP_005277989.1:p.Lys1397=
XM_006718478.2:c.5296A=	XP_006718541.1:p.Lys1766=
XM_011544854.1:c.5338A=	XP_011543156.1:p.Lys1780=
XM_011544855.1:c.5317A=	XP_011543157.1:p.Lys1773=
XM_011544856.1:c.5311A=	XP_011543158.1:p.Lys1771=
XM_011544857.1:c.5290A=	XP_011543159.1:p.Lys1764=
XM_011544859.1:c.4201A=	XP_011543161.1:p.Lys1401=
XM_005277932.3:c.4189A=	XP_005277989.1:p.Lys1397=
XM_017017387.1:c.5326A=	XP_016872876.1:p.Lys1776=
XM_017017388.1:c.5326A=	XP_016872877.1:p.Lys1776=
XM_017017389.1:c.5299A=	XP_016872878.1:p.Lys1767=
XM_017017390.1:c.3616A=	XP_016872879.1:p.Lys1206=
NM_133266.5:c.3562A=	NP_573573.2:p.Lys1188=
NR_110766.2:n.1181A=
NM_001379226.1:c.4189A=	NP_001366155.1:p.Lys1397=
NM_012309.5:c.5326A= MANE Select	NP_036441.2:p.Lys1776=