Canonical Allele Identifier: CA381682957

Gene: SHANK2

Linked Data

• MyVariant Identifiers: chr11:g.70332106A>G (hg19) ; chr11:g.70486001A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.70486001A>G , CM000673.2:g.70486001A>G	GRCh38
NC_000011.9:g.70332106A>G , CM000673.1:g.70332106A>G	GRCh37
NC_000011.8:g.70009754A>G	NCBI36
NG_042866.1:g.643796T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000338508.9:c.2525T>C	ENSP00000345193.7:p.Val842Ala
ENST00000412252.6:c.757+4302T>C	ENSP00000414876.2:n.757+4302T>C
ENST00000601538.6:c.4292T>C MANE Select	ENSP00000469689.2:p.Val1431Ala
ENST00000654939.1:c.1720T>C
ENST00000656230.1:c.3155T>C	ENSP00000499561.1:p.Val1052Ala
ENST00000659264.1:c.2582T>C	ENSP00000499270.1:p.Val861Ala
ENST00000338508.8:c.2528T>C	ENSP00000345193.6:p.Val843Ala
ENST00000357171.7:c.718+4302T>C	ENSP00000349694.4:n.718+4302T>C
ENST00000409161.5:c.2504T>C	ENSP00000386491.1:p.Val835Ala
ENST00000412252.5:c.755+4302T>C
ENST00000423696.6:c.3155T>C	ENSP00000394536.2:p.Val1052Ala
ENST00000424924.5:c.2129T>C	ENSP00000402944.1:p.Val710Ala
ENST00000449833.6:c.2528T>C	ENSP00000399423.3:p.Val843Ala
ENST00000601538.5:c.4292T>C	ENSP00000469689.2:p.Val1431Ala
NM_012309.4:c.4292T>C	NP_036441.2:p.Val1431Ala
NM_133266.4:c.2528T>C	NP_573573.2:p.Val843Ala
NR_110766.1:n.833+4302T>C
XM_005277930.2:c.4292T>C	XP_005277987.1:p.Val1431Ala
XM_005277932.2:c.3155T>C	XP_005277989.1:p.Val1052Ala
XM_006718478.2:c.4262T>C	XP_006718541.1:p.Val1421Ala
XM_011544854.1:c.4304T>C	XP_011543156.1:p.Val1435Ala
XM_011544855.1:c.4283T>C	XP_011543157.1:p.Val1428Ala
XM_011544856.1:c.4277T>C	XP_011543158.1:p.Val1426Ala
XM_011544857.1:c.4256T>C	XP_011543159.1:p.Val1419Ala
XM_011544858.1:c.4304T>C	XP_011543160.1:p.Val1435Ala
XM_011544859.1:c.3167T>C	XP_011543161.1:p.Val1056Ala
XM_005277932.3:c.3155T>C	XP_005277989.1:p.Val1052Ala
XM_017017387.1:c.4292T>C	XP_016872876.1:p.Val1431Ala
XM_017017388.1:c.4292T>C	XP_016872877.1:p.Val1431Ala
XM_017017389.1:c.4265T>C	XP_016872878.1:p.Val1422Ala
XM_017017390.1:c.2582T>C	XP_016872879.1:p.Val861Ala
NM_133266.5:c.2528T>C	NP_573573.2:p.Val843Ala
NR_110766.2:n.834+4302T>C
NM_001379226.1:c.3155T>C	NP_001366155.1:p.Val1052Ala
NM_012309.5:c.4292T>C MANE Select	NP_036441.2:p.Val1431Ala