Canonical Allele Identifier: CA381683071

Gene: SHANK2

Linked Data

• MyVariant Identifiers: chr11:g.70332121T>G (hg19) ; chr11:g.70486016T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.70486016T>G , CM000673.2:g.70486016T>G	GRCh38
NC_000011.9:g.70332121T>G , CM000673.1:g.70332121T>G	GRCh37
NC_000011.8:g.70009769T>G	NCBI36
NG_042866.1:g.643781A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338508.9:c.2510A>C	ENSP00000345193.7:p.Asp837Ala
ENST00000412252.6:c.757+4287A>C	ENSP00000414876.2:n.757+4287A>C
ENST00000601538.6:c.4277A>C MANE Select	ENSP00000469689.2:p.Asp1426Ala
ENST00000654939.1:c.1705A>C
ENST00000656230.1:c.3140A>C	ENSP00000499561.1:p.Asp1047Ala
ENST00000659264.1:c.2567A>C	ENSP00000499270.1:p.Asp856Ala
ENST00000338508.8:c.2513A>C	ENSP00000345193.6:p.Asp838Ala
ENST00000357171.7:c.718+4287A>C	ENSP00000349694.4:n.718+4287A>C
ENST00000409161.5:c.2489A>C	ENSP00000386491.1:p.Asp830Ala
ENST00000412252.5:c.755+4287A>C
ENST00000423696.6:c.3140A>C	ENSP00000394536.2:p.Asp1047Ala
ENST00000424924.5:c.2114A>C	ENSP00000402944.1:p.Asp705Ala
ENST00000449833.6:c.2513A>C	ENSP00000399423.3:p.Asp838Ala
ENST00000601538.5:c.4277A>C	ENSP00000469689.2:p.Asp1426Ala
NM_012309.4:c.4277A>C	NP_036441.2:p.Asp1426Ala
NM_133266.4:c.2513A>C	NP_573573.2:p.Asp838Ala
NR_110766.1:n.833+4287A>C
XM_005277930.2:c.4277A>C	XP_005277987.1:p.Asp1426Ala
XM_005277932.2:c.3140A>C	XP_005277989.1:p.Asp1047Ala
XM_006718478.2:c.4247A>C	XP_006718541.1:p.Asp1416Ala
XM_011544854.1:c.4289A>C	XP_011543156.1:p.Asp1430Ala
XM_011544855.1:c.4268A>C	XP_011543157.1:p.Asp1423Ala
XM_011544856.1:c.4262A>C	XP_011543158.1:p.Asp1421Ala
XM_011544857.1:c.4241A>C	XP_011543159.1:p.Asp1414Ala
XM_011544858.1:c.4289A>C	XP_011543160.1:p.Asp1430Ala
XM_011544859.1:c.3152A>C	XP_011543161.1:p.Asp1051Ala
XM_005277932.3:c.3140A>C	XP_005277989.1:p.Asp1047Ala
XM_017017387.1:c.4277A>C	XP_016872876.1:p.Asp1426Ala
XM_017017388.1:c.4277A>C	XP_016872877.1:p.Asp1426Ala
XM_017017389.1:c.4250A>C	XP_016872878.1:p.Asp1417Ala
XM_017017390.1:c.2567A>C	XP_016872879.1:p.Asp856Ala
NM_133266.5:c.2513A>C	NP_573573.2:p.Asp838Ala
NR_110766.2:n.834+4287A>C
NM_001379226.1:c.3140A>C	NP_001366155.1:p.Asp1047Ala
NM_012309.5:c.4277A>C MANE Select	NP_036441.2:p.Asp1426Ala