Canonical Allele Identifier: CA381675378

Gene: SHANK2

Linked Data

• MyVariant Identifiers: chr11:g.70319188G>C (hg19) ; chr11:g.70473083G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.70473083G>C , CM000673.2:g.70473083G>C	GRCh38
NC_000011.9:g.70319188G>C , CM000673.1:g.70319188G>C	GRCh37
NC_000011.8:g.69996836G>C	NCBI36
NG_042866.1:g.656714C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338508.9:c.3569C>G	ENSP00000345193.7:p.Thr1190Arg
ENST00000412252.6:c.1114C>G	ENSP00000414876.2:n.1114C>G
ENST00000601538.6:c.5336C>G MANE Select	ENSP00000469689.2:p.Thr1779Arg
ENST00000654939.1:c.2845C>G
ENST00000656230.1:c.4199C>G	ENSP00000499561.1:p.Thr1400Arg
ENST00000659264.1:c.3626C>G	ENSP00000499270.1:p.Thr1209Arg
ENST00000338508.8:c.3572C>G	ENSP00000345193.6:p.Thr1191Arg
ENST00000357171.7:c.*340C>G	ENSP00000349694.4:n.*340C>G
ENST00000409161.5:c.3548C>G	ENSP00000386491.1:p.Thr1183Arg
ENST00000412252.5:c.1112C>G
ENST00000423696.6:c.4199C>G	ENSP00000394536.2:p.Thr1400Arg
ENST00000424924.5:c.3173C>G	ENSP00000402944.1:p.Thr1058Arg
ENST00000449833.6:c.3572C>G	ENSP00000399423.3:p.Thr1191Arg
ENST00000601538.5:c.5336C>G	ENSP00000469689.2:p.Thr1779Arg
ENST00000606715.3:n.2088C>G
NM_012309.4:c.5336C>G	NP_036441.2:p.Thr1779Arg
NM_133266.4:c.3572C>G	NP_573573.2:p.Thr1191Arg
NR_110766.1:n.1190C>G
XM_005277930.2:c.5336C>G	XP_005277987.1:p.Thr1779Arg
XM_005277932.2:c.4199C>G	XP_005277989.1:p.Thr1400Arg
XM_006718478.2:c.5306C>G	XP_006718541.1:p.Thr1769Arg
XM_011544854.1:c.5348C>G	XP_011543156.1:p.Thr1783Arg
XM_011544855.1:c.5327C>G	XP_011543157.1:p.Thr1776Arg
XM_011544856.1:c.5321C>G	XP_011543158.1:p.Thr1774Arg
XM_011544857.1:c.5300C>G	XP_011543159.1:p.Thr1767Arg
XM_011544859.1:c.4211C>G	XP_011543161.1:p.Thr1404Arg
XM_005277932.3:c.4199C>G	XP_005277989.1:p.Thr1400Arg
XM_017017387.1:c.5336C>G	XP_016872876.1:p.Thr1779Arg
XM_017017388.1:c.5336C>G	XP_016872877.1:p.Thr1779Arg
XM_017017389.1:c.5309C>G	XP_016872878.1:p.Thr1770Arg
XM_017017390.1:c.3626C>G	XP_016872879.1:p.Thr1209Arg
NM_133266.5:c.3572C>G	NP_573573.2:p.Thr1191Arg
NR_110766.2:n.1191C>G
NM_001379226.1:c.4199C>G	NP_001366155.1:p.Thr1400Arg
NM_012309.5:c.5336C>G MANE Select	NP_036441.2:p.Thr1779Arg