Canonical Allele Identifier: CA381675424

Gene: SHANK2

Linked Data

• MyVariant Identifiers: chr11:g.70319195G>T (hg19) ; chr11:g.70473090G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.70473090G>T , CM000673.2:g.70473090G>T	GRCh38
NC_000011.9:g.70319195G>T , CM000673.1:g.70319195G>T	GRCh37
NC_000011.8:g.69996843G>T	NCBI36
NG_042866.1:g.656707C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338508.9:c.3562C>A	ENSP00000345193.7:p.Pro1188Thr
ENST00000412252.6:c.1107C>A	ENSP00000414876.2:n.1107C>A
ENST00000601538.6:c.5329C>A MANE Select	ENSP00000469689.2:p.Pro1777Thr
ENST00000654939.1:c.2838C>A
ENST00000656230.1:c.4192C>A	ENSP00000499561.1:p.Pro1398Thr
ENST00000659264.1:c.3619C>A	ENSP00000499270.1:p.Pro1207Thr
ENST00000338508.8:c.3565C>A	ENSP00000345193.6:p.Pro1189Thr
ENST00000357171.7:c.*333C>A	ENSP00000349694.4:n.*333C>A
ENST00000409161.5:c.3541C>A	ENSP00000386491.1:p.Pro1181Thr
ENST00000412252.5:c.1105C>A
ENST00000423696.6:c.4192C>A	ENSP00000394536.2:p.Pro1398Thr
ENST00000424924.5:c.3166C>A	ENSP00000402944.1:p.Pro1056Thr
ENST00000449833.6:c.3565C>A	ENSP00000399423.3:p.Pro1189Thr
ENST00000601538.5:c.5329C>A	ENSP00000469689.2:p.Pro1777Thr
ENST00000606715.3:n.2081C>A
NM_012309.4:c.5329C>A	NP_036441.2:p.Pro1777Thr
NM_133266.4:c.3565C>A	NP_573573.2:p.Pro1189Thr
NR_110766.1:n.1183C>A
XM_005277930.2:c.5329C>A	XP_005277987.1:p.Pro1777Thr
XM_005277932.2:c.4192C>A	XP_005277989.1:p.Pro1398Thr
XM_006718478.2:c.5299C>A	XP_006718541.1:p.Pro1767Thr
XM_011544854.1:c.5341C>A	XP_011543156.1:p.Pro1781Thr
XM_011544855.1:c.5320C>A	XP_011543157.1:p.Pro1774Thr
XM_011544856.1:c.5314C>A	XP_011543158.1:p.Pro1772Thr
XM_011544857.1:c.5293C>A	XP_011543159.1:p.Pro1765Thr
XM_011544859.1:c.4204C>A	XP_011543161.1:p.Pro1402Thr
XM_005277932.3:c.4192C>A	XP_005277989.1:p.Pro1398Thr
XM_017017387.1:c.5329C>A	XP_016872876.1:p.Pro1777Thr
XM_017017388.1:c.5329C>A	XP_016872877.1:p.Pro1777Thr
XM_017017389.1:c.5302C>A	XP_016872878.1:p.Pro1768Thr
XM_017017390.1:c.3619C>A	XP_016872879.1:p.Pro1207Thr
NM_133266.5:c.3565C>A	NP_573573.2:p.Pro1189Thr
NR_110766.2:n.1184C>A
NM_001379226.1:c.4192C>A	NP_001366155.1:p.Pro1398Thr
NM_012309.5:c.5329C>A MANE Select	NP_036441.2:p.Pro1777Thr