Canonical Allele Identifier: CA381676014

Gene: SHANK2

Linked Data

• MyVariant Identifiers: chr11:g.70319288G>A (hg19) ; chr11:g.70473183G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.70473183G>A , CM000673.2:g.70473183G>A	GRCh38
NC_000011.9:g.70319288G>A , CM000673.1:g.70319288G>A	GRCh37
NC_000011.8:g.69996936G>A	NCBI36
NG_042866.1:g.656614C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338508.9:c.3469C>T	ENSP00000345193.7:p.Gln1157Ter
ENST00000412252.6:c.1014C>T	ENSP00000414876.2:n.1014C>T
ENST00000601538.6:c.5236C>T MANE Select	ENSP00000469689.2:p.Gln1746Ter
ENST00000654939.1:c.2745C>T
ENST00000656230.1:c.4099C>T	ENSP00000499561.1:p.Gln1367Ter
ENST00000659264.1:c.3526C>T	ENSP00000499270.1:p.Gln1176Ter
ENST00000338508.8:c.3472C>T	ENSP00000345193.6:p.Gln1158Ter
ENST00000357171.7:c.*240C>T	ENSP00000349694.4:n.*240C>T
ENST00000409161.5:c.3448C>T	ENSP00000386491.1:p.Gln1150Ter
ENST00000412252.5:c.1012C>T
ENST00000423696.6:c.4099C>T	ENSP00000394536.2:p.Gln1367Ter
ENST00000424924.5:c.3073C>T	ENSP00000402944.1:p.Gln1025Ter
ENST00000449833.6:c.3472C>T	ENSP00000399423.3:p.Gln1158Ter
ENST00000601538.5:c.5236C>T	ENSP00000469689.2:p.Gln1746Ter
ENST00000606715.3:n.1988C>T
NM_012309.4:c.5236C>T	NP_036441.2:p.Gln1746Ter
NM_133266.4:c.3472C>T	NP_573573.2:p.Gln1158Ter
NR_110766.1:n.1090C>T
XM_005277930.2:c.5236C>T	XP_005277987.1:p.Gln1746Ter
XM_005277932.2:c.4099C>T	XP_005277989.1:p.Gln1367Ter
XM_006718478.2:c.5206C>T	XP_006718541.1:p.Gln1736Ter
XM_011544854.1:c.5248C>T	XP_011543156.1:p.Gln1750Ter
XM_011544855.1:c.5227C>T	XP_011543157.1:p.Gln1743Ter
XM_011544856.1:c.5221C>T	XP_011543158.1:p.Gln1741Ter
XM_011544857.1:c.5200C>T	XP_011543159.1:p.Gln1734Ter
XM_011544859.1:c.4111C>T	XP_011543161.1:p.Gln1371Ter
XM_005277932.3:c.4099C>T	XP_005277989.1:p.Gln1367Ter
XM_017017387.1:c.5236C>T	XP_016872876.1:p.Gln1746Ter
XM_017017388.1:c.5236C>T	XP_016872877.1:p.Gln1746Ter
XM_017017389.1:c.5209C>T	XP_016872878.1:p.Gln1737Ter
XM_017017390.1:c.3526C>T	XP_016872879.1:p.Gln1176Ter
NM_133266.5:c.3472C>T	NP_573573.2:p.Gln1158Ter
NR_110766.2:n.1091C>T
NM_001379226.1:c.4099C>T	NP_001366155.1:p.Gln1367Ter
NM_012309.5:c.5236C>T MANE Select	NP_036441.2:p.Gln1746Ter