Canonical Allele Identifier: CA381676213

Gene: SHANK2

Linked Data

• MyVariant Identifiers: chr11:g.70319335G>T (hg19) ; chr11:g.70473230G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.70473230G>T , CM000673.2:g.70473230G>T	GRCh38
NC_000011.9:g.70319335G>T , CM000673.1:g.70319335G>T	GRCh37
NC_000011.8:g.69996983G>T	NCBI36
NG_042866.1:g.656567C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338508.9:c.3422C>A	ENSP00000345193.7:p.Thr1141Asn
ENST00000412252.6:c.967C>A	ENSP00000414876.2:n.967C>A
ENST00000601538.6:c.5189C>A MANE Select	ENSP00000469689.2:p.Thr1730Asn
ENST00000654939.1:c.2698C>A
ENST00000656230.1:c.4052C>A	ENSP00000499561.1:p.Thr1351Asn
ENST00000659264.1:c.3479C>A	ENSP00000499270.1:p.Thr1160Asn
ENST00000338508.8:c.3425C>A	ENSP00000345193.6:p.Thr1142Asn
ENST00000357171.7:c.*193C>A	ENSP00000349694.4:n.*193C>A
ENST00000409161.5:c.3401C>A	ENSP00000386491.1:p.Thr1134Asn
ENST00000412252.5:c.965C>A
ENST00000423696.6:c.4052C>A	ENSP00000394536.2:p.Thr1351Asn
ENST00000424924.5:c.3026C>A	ENSP00000402944.1:p.Thr1009Asn
ENST00000449833.6:c.3425C>A	ENSP00000399423.3:p.Thr1142Asn
ENST00000601538.5:c.5189C>A	ENSP00000469689.2:p.Thr1730Asn
ENST00000606715.3:n.1941C>A
NM_012309.4:c.5189C>A	NP_036441.2:p.Thr1730Asn
NM_133266.4:c.3425C>A	NP_573573.2:p.Thr1142Asn
NR_110766.1:n.1043C>A
XM_005277930.2:c.5189C>A	XP_005277987.1:p.Thr1730Asn
XM_005277932.2:c.4052C>A	XP_005277989.1:p.Thr1351Asn
XM_006718478.2:c.5159C>A	XP_006718541.1:p.Thr1720Asn
XM_011544854.1:c.5201C>A	XP_011543156.1:p.Thr1734Asn
XM_011544855.1:c.5180C>A	XP_011543157.1:p.Thr1727Asn
XM_011544856.1:c.5174C>A	XP_011543158.1:p.Thr1725Asn
XM_011544857.1:c.5153C>A	XP_011543159.1:p.Thr1718Asn
XM_011544859.1:c.4064C>A	XP_011543161.1:p.Thr1355Asn
XM_005277932.3:c.4052C>A	XP_005277989.1:p.Thr1351Asn
XM_017017387.1:c.5189C>A	XP_016872876.1:p.Thr1730Asn
XM_017017388.1:c.5189C>A	XP_016872877.1:p.Thr1730Asn
XM_017017389.1:c.5162C>A	XP_016872878.1:p.Thr1721Asn
XM_017017390.1:c.3479C>A	XP_016872879.1:p.Thr1160Asn
NM_133266.5:c.3425C>A	NP_573573.2:p.Thr1142Asn
NR_110766.2:n.1044C>A
NM_001379226.1:c.4052C>A	NP_001366155.1:p.Thr1351Asn
NM_012309.5:c.5189C>A MANE Select	NP_036441.2:p.Thr1730Asn