Canonical Allele Identifier: CA381683056

Gene: SHANK2

Linked Data

• gnomAD v4: 11-70486014-G-C
• MyVariant Identifiers: chr11:g.70332119G>C (hg19) ; chr11:g.70486014G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.70486014G>C , CM000673.2:g.70486014G>C	GRCh38
NC_000011.9:g.70332119G>C , CM000673.1:g.70332119G>C	GRCh37
NC_000011.8:g.70009767G>C	NCBI36
NG_042866.1:g.643783C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338508.9:c.2512C>G	ENSP00000345193.7:p.Arg838Gly
ENST00000412252.6:c.757+4289C>G	ENSP00000414876.2:n.757+4289C>G
ENST00000601538.6:c.4279C>G MANE Select	ENSP00000469689.2:p.Arg1427Gly
ENST00000654939.1:c.1707C>G
ENST00000656230.1:c.3142C>G	ENSP00000499561.1:p.Arg1048Gly
ENST00000659264.1:c.2569C>G	ENSP00000499270.1:p.Arg857Gly
ENST00000338508.8:c.2515C>G	ENSP00000345193.6:p.Arg839Gly
ENST00000357171.7:c.718+4289C>G	ENSP00000349694.4:n.718+4289C>G
ENST00000409161.5:c.2491C>G	ENSP00000386491.1:p.Arg831Gly
ENST00000412252.5:c.755+4289C>G
ENST00000423696.6:c.3142C>G	ENSP00000394536.2:p.Arg1048Gly
ENST00000424924.5:c.2116C>G	ENSP00000402944.1:p.Arg706Gly
ENST00000449833.6:c.2515C>G	ENSP00000399423.3:p.Arg839Gly
ENST00000601538.5:c.4279C>G	ENSP00000469689.2:p.Arg1427Gly
NM_012309.4:c.4279C>G	NP_036441.2:p.Arg1427Gly
NM_133266.4:c.2515C>G	NP_573573.2:p.Arg839Gly
NR_110766.1:n.833+4289C>G
XM_005277930.2:c.4279C>G	XP_005277987.1:p.Arg1427Gly
XM_005277932.2:c.3142C>G	XP_005277989.1:p.Arg1048Gly
XM_006718478.2:c.4249C>G	XP_006718541.1:p.Arg1417Gly
XM_011544854.1:c.4291C>G	XP_011543156.1:p.Arg1431Gly
XM_011544855.1:c.4270C>G	XP_011543157.1:p.Arg1424Gly
XM_011544856.1:c.4264C>G	XP_011543158.1:p.Arg1422Gly
XM_011544857.1:c.4243C>G	XP_011543159.1:p.Arg1415Gly
XM_011544858.1:c.4291C>G	XP_011543160.1:p.Arg1431Gly
XM_011544859.1:c.3154C>G	XP_011543161.1:p.Arg1052Gly
XM_005277932.3:c.3142C>G	XP_005277989.1:p.Arg1048Gly
XM_017017387.1:c.4279C>G	XP_016872876.1:p.Arg1427Gly
XM_017017388.1:c.4279C>G	XP_016872877.1:p.Arg1427Gly
XM_017017389.1:c.4252C>G	XP_016872878.1:p.Arg1418Gly
XM_017017390.1:c.2569C>G	XP_016872879.1:p.Arg857Gly
NM_133266.5:c.2515C>G	NP_573573.2:p.Arg839Gly
NR_110766.2:n.834+4289C>G
NM_001379226.1:c.3142C>G	NP_001366155.1:p.Arg1048Gly
NM_012309.5:c.4279C>G MANE Select	NP_036441.2:p.Arg1427Gly