Canonical Allele Identifier: CA1651267253

Gene: GRIK2

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.101879428T>G , CM000668.2:g.101879428T>G	GRCh38
NC_000006.11:g.102327303T>G , CM000668.1:g.102327303T>G	GRCh37
NC_000006.10:g.102433996T>G	NCBI36
NG_009224.2:g.485399T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436862.2:c.*569-10212T>G	ENSP00000407140.2:n.*569-10212T>G
ENST00000681975.1:c.1525-10212T>G	ENSP00000508014.1:n.1525-10212T>G
ENST00000682052.1:n.1910-10212T>G
ENST00000682090.1:c.1525-10212T>G	ENSP00000508130.1:n.1525-10212T>G
ENST00000682115.1:c.1525-10212T>G	ENSP00000508069.1:n.1525-10212T>G
ENST00000682222.1:c.1525-10212T>G	ENSP00000506840.1:n.1525-10212T>G
ENST00000682716.1:n.1910-10212T>G
ENST00000682823.1:n.2320T>G
ENST00000683208.1:c.*135+264T>G	ENSP00000508151.1:n.*135+264T>G
ENST00000683215.1:c.1525-10212T>G	ENSP00000507424.1:n.1525-10212T>G
ENST00000683774.1:n.2166-10212T>G
ENST00000683806.1:c.*1552-10212T>G	ENSP00000506783.1:n.*1552-10212T>G
ENST00000683903.1:c.1297-10212T>G	ENSP00000507071.1:n.1297-10212T>G
ENST00000684027.1:c.*328-10212T>G	ENSP00000508056.1:n.*328-10212T>G
ENST00000684068.1:c.1525-10212T>G	ENSP00000508175.1:n.1525-10212T>G
ENST00000684279.1:n.1910-10212T>G
ENST00000684518.1:c.*569-10212T>G	ENSP00000507289.1:n.*569-10212T>G
ENST00000369134.9:c.1525-10212T>G MANE Select	ENSP00000358130.6:n.1525-10212T>G
ENST00000369137.8:c.*1516-10212T>G	ENSP00000358133.5:n.*1516-10212T>G
ENST00000421544.6:c.1525-10212T>G	ENSP00000397026.1:n.1525-10212T>G
ENST00000318991.10:c.1411-10212T>G	ENSP00000313276.7:n.1411-10212T>G
ENST00000369134.8:c.1411-10212T>G	ENSP00000358130.5:n.1411-10212T>G
ENST00000369137.7:c.1411-10212T>G	ENSP00000358133.4:n.1411-10212T>G
ENST00000369138.5:c.1525-10212T>G	ENSP00000358134.1:n.1525-10212T>G
ENST00000413795.5:c.1525-10212T>G	ENSP00000405596.1:n.1525-10212T>G
ENST00000421544.5:c.1525-10212T>G	ENSP00000397026.1:n.1525-10212T>G
ENST00000436862.1:c.322-10212T>G	ENSP00000407140.1:n.322-10212T>G
NM_001166247.1:c.1525-10212T>G	NP_001159719.1:n.1525-10212T>G
NM_021956.4:c.1525-10212T>G	NP_068775.1:n.1525-10212T>G
NM_175768.3:c.1525-10212T>G	NP_786944.1:n.1525-10212T>G
XM_005266945.2:c.1525-10212T>G	XP_005267002.1:n.1525-10212T>G
XM_005266946.2:c.1378-10212T>G	XP_005267003.1:n.1378-10212T>G
XM_011535777.1:c.1525-10212T>G	XP_011534079.1:n.1525-10212T>G
XM_011535778.1:c.1525-10212T>G	XP_011534080.1:n.1525-10212T>G
XM_011535779.1:c.1525-10212T>G	XP_011534081.1:n.1525-10212T>G
XM_011535780.1:c.1525-10212T>G	XP_011534082.1:n.1525-10212T>G
XM_011535781.1:c.1525-10212T>G	XP_011534083.1:n.1525-10212T>G
XM_005266946.4:c.1378-10212T>G	XP_005267003.1:n.1378-10212T>G
XM_011535777.3:c.1525-10212T>G	XP_011534079.1:n.1525-10212T>G
XM_017010781.2:c.1525-10212T>G	XP_016866270.1:n.1525-10212T>G
XM_017010782.2:c.1525-10212T>G	XP_016866271.1:n.1525-10212T>G
XM_024446410.1:c.1525-10212T>G	XP_024302178.1:n.1525-10212T>G
XM_024446411.1:c.1525-10212T>G	XP_024302179.1:n.1525-10212T>G
XR_002956278.1:n.1948-10212T>G
NM_021956.5:c.1525-10212T>G MANE Select	NP_068775.1:n.1525-10212T>G