Canonical Allele Identifier: CA475471088

Gene: SHANK2

Linked Data

• gnomAD v4: 11-70473109-T-C
• MyVariant Identifiers: chr11:g.70319214T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.70473109T>C , CM000673.2:g.70473109T>C	GRCh38
NC_000011.9:g.70319214T>C , CM000673.1:g.70319214T>C	GRCh37
NC_000011.8:g.69996862T>C	NCBI36
NG_042866.1:g.656688A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338508.9:c.3543A>G	ENSP00000345193.7:p.Gln1181=
ENST00000412252.6:c.1088A>G	ENSP00000414876.2:n.1088A>G
ENST00000601538.6:c.5310A>G MANE Select	ENSP00000469689.2:p.Gln1770=
ENST00000654939.1:c.2819A>G
ENST00000656230.1:c.4173A>G	ENSP00000499561.1:p.Gln1391=
ENST00000659264.1:c.3600A>G	ENSP00000499270.1:p.Gln1200=
ENST00000338508.8:c.3546A>G	ENSP00000345193.6:p.Gln1182=
ENST00000357171.7:c.*314A>G	ENSP00000349694.4:n.*314A>G
ENST00000409161.5:c.3522A>G	ENSP00000386491.1:p.Gln1174=
ENST00000412252.5:c.1086A>G
ENST00000423696.6:c.4173A>G	ENSP00000394536.2:p.Gln1391=
ENST00000424924.5:c.3147A>G	ENSP00000402944.1:p.Gln1049=
ENST00000449833.6:c.3546A>G	ENSP00000399423.3:p.Gln1182=
ENST00000601538.5:c.5310A>G	ENSP00000469689.2:p.Gln1770=
ENST00000606715.3:n.2062A>G
NM_012309.4:c.5310A>G	NP_036441.2:p.Gln1770=
NM_133266.4:c.3546A>G	NP_573573.2:p.Gln1182=
NR_110766.1:n.1164A>G
XM_005277930.2:c.5310A>G	XP_005277987.1:p.Gln1770=
XM_005277932.2:c.4173A>G	XP_005277989.1:p.Gln1391=
XM_006718478.2:c.5280A>G	XP_006718541.1:p.Gln1760=
XM_011544854.1:c.5322A>G	XP_011543156.1:p.Gln1774=
XM_011544855.1:c.5301A>G	XP_011543157.1:p.Gln1767=
XM_011544856.1:c.5295A>G	XP_011543158.1:p.Gln1765=
XM_011544857.1:c.5274A>G	XP_011543159.1:p.Gln1758=
XM_011544859.1:c.4185A>G	XP_011543161.1:p.Gln1395=
XM_005277932.3:c.4173A>G	XP_005277989.1:p.Gln1391=
XM_017017387.1:c.5310A>G	XP_016872876.1:p.Gln1770=
XM_017017388.1:c.5310A>G	XP_016872877.1:p.Gln1770=
XM_017017389.1:c.5283A>G	XP_016872878.1:p.Gln1761=
XM_017017390.1:c.3600A>G	XP_016872879.1:p.Gln1200=
NM_133266.5:c.3546A>G	NP_573573.2:p.Gln1182=
NR_110766.2:n.1165A>G
NM_001379226.1:c.4173A>G	NP_001366155.1:p.Gln1391=
NM_012309.5:c.5310A>G MANE Select	NP_036441.2:p.Gln1770=