Canonical Allele Identifier: CA381675373

Gene: SHANK2

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338508.9:c.3569C>A	ENSP00000345193.7:p.Thr1190Lys
ENST00000412252.6:c.1114C>A	ENSP00000414876.2:n.1114C>A
ENST00000601538.6:c.5336C>A MANE Select	ENSP00000469689.2:p.Thr1779Lys
ENST00000654939.1:c.2845C>A
ENST00000656230.1:c.4199C>A	ENSP00000499561.1:p.Thr1400Lys
ENST00000659264.1:c.3626C>A	ENSP00000499270.1:p.Thr1209Lys
ENST00000338508.8:c.3572C>A	ENSP00000345193.6:p.Thr1191Lys
ENST00000357171.7:c.*340C>A	ENSP00000349694.4:n.*340C>A
ENST00000409161.5:c.3548C>A	ENSP00000386491.1:p.Thr1183Lys
ENST00000412252.5:c.1112C>A
ENST00000423696.6:c.4199C>A	ENSP00000394536.2:p.Thr1400Lys
ENST00000424924.5:c.3173C>A	ENSP00000402944.1:p.Thr1058Lys
ENST00000449833.6:c.3572C>A	ENSP00000399423.3:p.Thr1191Lys
ENST00000601538.5:c.5336C>A	ENSP00000469689.2:p.Thr1779Lys
ENST00000606715.3:n.2088C>A
NM_012309.4:c.5336C>A	NP_036441.2:p.Thr1779Lys
NM_133266.4:c.3572C>A	NP_573573.2:p.Thr1191Lys
NR_110766.1:n.1190C>A
XM_005277930.2:c.5336C>A	XP_005277987.1:p.Thr1779Lys
XM_005277932.2:c.4199C>A	XP_005277989.1:p.Thr1400Lys
XM_006718478.2:c.5306C>A	XP_006718541.1:p.Thr1769Lys
XM_011544854.1:c.5348C>A	XP_011543156.1:p.Thr1783Lys
XM_011544855.1:c.5327C>A	XP_011543157.1:p.Thr1776Lys
XM_011544856.1:c.5321C>A	XP_011543158.1:p.Thr1774Lys
XM_011544857.1:c.5300C>A	XP_011543159.1:p.Thr1767Lys
XM_011544859.1:c.4211C>A	XP_011543161.1:p.Thr1404Lys
XM_005277932.3:c.4199C>A	XP_005277989.1:p.Thr1400Lys
XM_017017387.1:c.5336C>A	XP_016872876.1:p.Thr1779Lys
XM_017017388.1:c.5336C>A	XP_016872877.1:p.Thr1779Lys
XM_017017389.1:c.5309C>A	XP_016872878.1:p.Thr1770Lys
XM_017017390.1:c.3626C>A	XP_016872879.1:p.Thr1209Lys
NM_133266.5:c.3572C>A	NP_573573.2:p.Thr1191Lys
NR_110766.2:n.1191C>A
NM_001379226.1:c.4199C>A	NP_001366155.1:p.Thr1400Lys
NM_012309.5:c.5336C>A MANE Select	NP_036441.2:p.Thr1779Lys