Canonical Allele Identifier: CA381675646

Gene: SHANK2

Linked Data

• MyVariant Identifiers: chr11:g.70319222T>C (hg19) ; chr11:g.70473117T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.70473117T>C , CM000673.2:g.70473117T>C	GRCh38
NC_000011.9:g.70319222T>C , CM000673.1:g.70319222T>C	GRCh37
NC_000011.8:g.69996870T>C	NCBI36
NG_042866.1:g.656680A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338508.9:c.3535A>G	ENSP00000345193.7:p.Ile1179Val
ENST00000412252.6:c.1080A>G	ENSP00000414876.2:n.1080A>G
ENST00000601538.6:c.5302A>G MANE Select	ENSP00000469689.2:p.Ile1768Val
ENST00000654939.1:c.2811A>G
ENST00000656230.1:c.4165A>G	ENSP00000499561.1:p.Ile1389Val
ENST00000659264.1:c.3592A>G	ENSP00000499270.1:p.Ile1198Val
ENST00000338508.8:c.3538A>G	ENSP00000345193.6:p.Ile1180Val
ENST00000357171.7:c.*306A>G	ENSP00000349694.4:n.*306A>G
ENST00000409161.5:c.3514A>G	ENSP00000386491.1:p.Ile1172Val
ENST00000412252.5:c.1078A>G
ENST00000423696.6:c.4165A>G	ENSP00000394536.2:p.Ile1389Val
ENST00000424924.5:c.3139A>G	ENSP00000402944.1:p.Ile1047Val
ENST00000449833.6:c.3538A>G	ENSP00000399423.3:p.Ile1180Val
ENST00000601538.5:c.5302A>G	ENSP00000469689.2:p.Ile1768Val
ENST00000606715.3:n.2054A>G
NM_012309.4:c.5302A>G	NP_036441.2:p.Ile1768Val
NM_133266.4:c.3538A>G	NP_573573.2:p.Ile1180Val
NR_110766.1:n.1156A>G
XM_005277930.2:c.5302A>G	XP_005277987.1:p.Ile1768Val
XM_005277932.2:c.4165A>G	XP_005277989.1:p.Ile1389Val
XM_006718478.2:c.5272A>G	XP_006718541.1:p.Ile1758Val
XM_011544854.1:c.5314A>G	XP_011543156.1:p.Ile1772Val
XM_011544855.1:c.5293A>G	XP_011543157.1:p.Ile1765Val
XM_011544856.1:c.5287A>G	XP_011543158.1:p.Ile1763Val
XM_011544857.1:c.5266A>G	XP_011543159.1:p.Ile1756Val
XM_011544859.1:c.4177A>G	XP_011543161.1:p.Ile1393Val
XM_005277932.3:c.4165A>G	XP_005277989.1:p.Ile1389Val
XM_017017387.1:c.5302A>G	XP_016872876.1:p.Ile1768Val
XM_017017388.1:c.5302A>G	XP_016872877.1:p.Ile1768Val
XM_017017389.1:c.5275A>G	XP_016872878.1:p.Ile1759Val
XM_017017390.1:c.3592A>G	XP_016872879.1:p.Ile1198Val
NM_133266.5:c.3538A>G	NP_573573.2:p.Ile1180Val
NR_110766.2:n.1157A>G
NM_001379226.1:c.4165A>G	NP_001366155.1:p.Ile1389Val
NM_012309.5:c.5302A>G MANE Select	NP_036441.2:p.Ile1768Val