Canonical Allele Identifier: CA224326261

Gene: SHANK2

Linked Data

• dbSNP Id: rs1005220908
• MyVariant Identifiers: chr11:g.71084249G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.71084249G>A , CM000673.2:g.71084249G>A	GRCh38
NG_042866.1:g.145548C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000601538.6:c.912+8173C>T MANE Select	ENSP00000469689.2:n.912+8173C>T
ENST00000458632.2:c.320+8173C>T
ENST00000601538.5:c.912+8173C>T	ENSP00000469689.2:n.912+8173C>T
ENST00000608988.5:c.*475+8173C>T	ENSP00000476264.2:n.*475+8173C>T
ENST00000618363.4:c.56+8173C>T
NM_012309.4:c.912+8173C>T	NP_036441.2:n.912+8173C>T
XM_005277930.2:c.912+8173C>T	XP_005277987.1:n.912+8173C>T
XM_006718478.2:c.912+8173C>T	XP_006718541.1:n.912+8173C>T
XM_011544854.1:c.912+8173C>T	XP_011543156.1:n.912+8173C>T
XM_011544855.1:c.912+8173C>T	XP_011543157.1:n.912+8173C>T
XM_011544856.1:c.912+8173C>T	XP_011543158.1:n.912+8173C>T
XM_011544857.1:c.912+8173C>T	XP_011543159.1:n.912+8173C>T
XM_011544858.1:c.912+8173C>T	XP_011543160.1:n.912+8173C>T
XM_017017387.1:c.912+8173C>T	XP_016872876.1:n.912+8173C>T
XM_017017388.1:c.912+8173C>T	XP_016872877.1:n.912+8173C>T
XM_017017389.1:c.912+8173C>T	XP_016872878.1:n.912+8173C>T
NM_012309.5:c.912+8173C>T MANE Select	NP_036441.2:n.912+8173C>T