Canonical Allele Identifier: CA381683170

Gene: SHANK2

Linked Data

• MyVariant Identifiers: chr11:g.70332136A>C (hg19) ; chr11:g.70486031A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.70486031A>C , CM000673.2:g.70486031A>C	GRCh38
NC_000011.9:g.70332136A>C , CM000673.1:g.70332136A>C	GRCh37
NC_000011.8:g.70009784A>C	NCBI36
NG_042866.1:g.643766T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338508.9:c.2495T>G	ENSP00000345193.7:p.Phe832Cys
ENST00000412252.6:c.757+4272T>G	ENSP00000414876.2:n.757+4272T>G
ENST00000601538.6:c.4262T>G MANE Select	ENSP00000469689.2:p.Phe1421Cys
ENST00000654939.1:c.1690T>G
ENST00000656230.1:c.3125T>G	ENSP00000499561.1:p.Phe1042Cys
ENST00000659264.1:c.2552T>G	ENSP00000499270.1:p.Phe851Cys
ENST00000338508.8:c.2498T>G	ENSP00000345193.6:p.Phe833Cys
ENST00000357171.7:c.718+4272T>G	ENSP00000349694.4:n.718+4272T>G
ENST00000409161.5:c.2474T>G	ENSP00000386491.1:p.Phe825Cys
ENST00000412252.5:c.755+4272T>G
ENST00000423696.6:c.3125T>G	ENSP00000394536.2:p.Phe1042Cys
ENST00000424924.5:c.2099T>G	ENSP00000402944.1:p.Phe700Cys
ENST00000449833.6:c.2498T>G	ENSP00000399423.3:p.Phe833Cys
ENST00000601538.5:c.4262T>G	ENSP00000469689.2:p.Phe1421Cys
NM_012309.4:c.4262T>G	NP_036441.2:p.Phe1421Cys
NM_133266.4:c.2498T>G	NP_573573.2:p.Phe833Cys
NR_110766.1:n.833+4272T>G
XM_005277930.2:c.4262T>G	XP_005277987.1:p.Phe1421Cys
XM_005277932.2:c.3125T>G	XP_005277989.1:p.Phe1042Cys
XM_006718478.2:c.4232T>G	XP_006718541.1:p.Phe1411Cys
XM_011544854.1:c.4274T>G	XP_011543156.1:p.Phe1425Cys
XM_011544855.1:c.4253T>G	XP_011543157.1:p.Phe1418Cys
XM_011544856.1:c.4247T>G	XP_011543158.1:p.Phe1416Cys
XM_011544857.1:c.4226T>G	XP_011543159.1:p.Phe1409Cys
XM_011544858.1:c.4274T>G	XP_011543160.1:p.Phe1425Cys
XM_011544859.1:c.3137T>G	XP_011543161.1:p.Phe1046Cys
XM_005277932.3:c.3125T>G	XP_005277989.1:p.Phe1042Cys
XM_017017387.1:c.4262T>G	XP_016872876.1:p.Phe1421Cys
XM_017017388.1:c.4262T>G	XP_016872877.1:p.Phe1421Cys
XM_017017389.1:c.4235T>G	XP_016872878.1:p.Phe1412Cys
XM_017017390.1:c.2552T>G	XP_016872879.1:p.Phe851Cys
NM_133266.5:c.2498T>G	NP_573573.2:p.Phe833Cys
NR_110766.2:n.834+4272T>G
NM_001379226.1:c.3125T>G	NP_001366155.1:p.Phe1042Cys
NM_012309.5:c.4262T>G MANE Select	NP_036441.2:p.Phe1421Cys