Canonical Allele Identifier: CA381676190

Gene: SHANK2

Linked Data

• MyVariant Identifiers: chr11:g.70319326G>T (hg19) ; chr11:g.70473221G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.70473221G>T , CM000673.2:g.70473221G>T	GRCh38
NC_000011.9:g.70319326G>T , CM000673.1:g.70319326G>T	GRCh37
NC_000011.8:g.69996974G>T	NCBI36
NG_042866.1:g.656576C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338508.9:c.3431C>A	ENSP00000345193.7:p.Pro1144His
ENST00000412252.6:c.976C>A	ENSP00000414876.2:n.976C>A
ENST00000601538.6:c.5198C>A MANE Select	ENSP00000469689.2:p.Pro1733His
ENST00000654939.1:c.2707C>A
ENST00000656230.1:c.4061C>A	ENSP00000499561.1:p.Pro1354His
ENST00000659264.1:c.3488C>A	ENSP00000499270.1:p.Pro1163His
ENST00000338508.8:c.3434C>A	ENSP00000345193.6:p.Pro1145His
ENST00000357171.7:c.*202C>A	ENSP00000349694.4:n.*202C>A
ENST00000409161.5:c.3410C>A	ENSP00000386491.1:p.Pro1137His
ENST00000412252.5:c.974C>A
ENST00000423696.6:c.4061C>A	ENSP00000394536.2:p.Pro1354His
ENST00000424924.5:c.3035C>A	ENSP00000402944.1:p.Pro1012His
ENST00000449833.6:c.3434C>A	ENSP00000399423.3:p.Pro1145His
ENST00000601538.5:c.5198C>A	ENSP00000469689.2:p.Pro1733His
ENST00000606715.3:n.1950C>A
NM_012309.4:c.5198C>A	NP_036441.2:p.Pro1733His
NM_133266.4:c.3434C>A	NP_573573.2:p.Pro1145His
NR_110766.1:n.1052C>A
XM_005277930.2:c.5198C>A	XP_005277987.1:p.Pro1733His
XM_005277932.2:c.4061C>A	XP_005277989.1:p.Pro1354His
XM_006718478.2:c.5168C>A	XP_006718541.1:p.Pro1723His
XM_011544854.1:c.5210C>A	XP_011543156.1:p.Pro1737His
XM_011544855.1:c.5189C>A	XP_011543157.1:p.Pro1730His
XM_011544856.1:c.5183C>A	XP_011543158.1:p.Pro1728His
XM_011544857.1:c.5162C>A	XP_011543159.1:p.Pro1721His
XM_011544859.1:c.4073C>A	XP_011543161.1:p.Pro1358His
XM_005277932.3:c.4061C>A	XP_005277989.1:p.Pro1354His
XM_017017387.1:c.5198C>A	XP_016872876.1:p.Pro1733His
XM_017017388.1:c.5198C>A	XP_016872877.1:p.Pro1733His
XM_017017389.1:c.5171C>A	XP_016872878.1:p.Pro1724His
XM_017017390.1:c.3488C>A	XP_016872879.1:p.Pro1163His
NM_133266.5:c.3434C>A	NP_573573.2:p.Pro1145His
NR_110766.2:n.1053C>A
NM_001379226.1:c.4061C>A	NP_001366155.1:p.Pro1354His
NM_012309.5:c.5198C>A MANE Select	NP_036441.2:p.Pro1733His