Canonical Allele Identifier: CA381675484

Gene: SHANK2

Linked Data

• MyVariant Identifiers: chr11:g.70319203G>C (hg19) ; chr11:g.70473098G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.70473098G>C , CM000673.2:g.70473098G>C	GRCh38
NC_000011.9:g.70319203G>C , CM000673.1:g.70319203G>C	GRCh37
NC_000011.8:g.69996851G>C	NCBI36
NG_042866.1:g.656699C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338508.9:c.3554C>G	ENSP00000345193.7:p.Ser1185Ter
ENST00000412252.6:c.1099C>G	ENSP00000414876.2:n.1099C>G
ENST00000601538.6:c.5321C>G MANE Select	ENSP00000469689.2:p.Ser1774Ter
ENST00000654939.1:c.2830C>G
ENST00000656230.1:c.4184C>G	ENSP00000499561.1:p.Ser1395Ter
ENST00000659264.1:c.3611C>G	ENSP00000499270.1:p.Ser1204Ter
ENST00000338508.8:c.3557C>G	ENSP00000345193.6:p.Ser1186Ter
ENST00000357171.7:c.*325C>G	ENSP00000349694.4:n.*325C>G
ENST00000409161.5:c.3533C>G	ENSP00000386491.1:p.Ser1178Ter
ENST00000412252.5:c.1097C>G
ENST00000423696.6:c.4184C>G	ENSP00000394536.2:p.Ser1395Ter
ENST00000424924.5:c.3158C>G	ENSP00000402944.1:p.Ser1053Ter
ENST00000449833.6:c.3557C>G	ENSP00000399423.3:p.Ser1186Ter
ENST00000601538.5:c.5321C>G	ENSP00000469689.2:p.Ser1774Ter
ENST00000606715.3:n.2073C>G
NM_012309.4:c.5321C>G	NP_036441.2:p.Ser1774Ter
NM_133266.4:c.3557C>G	NP_573573.2:p.Ser1186Ter
NR_110766.1:n.1175C>G
XM_005277930.2:c.5321C>G	XP_005277987.1:p.Ser1774Ter
XM_005277932.2:c.4184C>G	XP_005277989.1:p.Ser1395Ter
XM_006718478.2:c.5291C>G	XP_006718541.1:p.Ser1764Ter
XM_011544854.1:c.5333C>G	XP_011543156.1:p.Ser1778Ter
XM_011544855.1:c.5312C>G	XP_011543157.1:p.Ser1771Ter
XM_011544856.1:c.5306C>G	XP_011543158.1:p.Ser1769Ter
XM_011544857.1:c.5285C>G	XP_011543159.1:p.Ser1762Ter
XM_011544859.1:c.4196C>G	XP_011543161.1:p.Ser1399Ter
XM_005277932.3:c.4184C>G	XP_005277989.1:p.Ser1395Ter
XM_017017387.1:c.5321C>G	XP_016872876.1:p.Ser1774Ter
XM_017017388.1:c.5321C>G	XP_016872877.1:p.Ser1774Ter
XM_017017389.1:c.5294C>G	XP_016872878.1:p.Ser1765Ter
XM_017017390.1:c.3611C>G	XP_016872879.1:p.Ser1204Ter
NM_133266.5:c.3557C>G	NP_573573.2:p.Ser1186Ter
NR_110766.2:n.1176C>G
NM_001379226.1:c.4184C>G	NP_001366155.1:p.Ser1395Ter
NM_012309.5:c.5321C>G MANE Select	NP_036441.2:p.Ser1774Ter