Canonical Allele Identifier: CA816364337

Gene: GRIK2

Linked Data

• dbSNP Id: rs1556995
• MyVariant Identifiers: chr6:g.102317345C>A (hg19) ; chr6:g.101869470C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.101869470C>A , CM000668.2:g.101869470C>A	GRCh38
NC_000006.11:g.102317345C>A , CM000668.1:g.102317345C>A	GRCh37
NC_000006.10:g.102424038C>A	NCBI36
NG_009224.2:g.475441C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000436862.2:c.*568+9977C>A	ENSP00000407140.2:n.*568+9977C>A
ENST00000681975.1:c.1524+9977C>A	ENSP00000508014.1:n.1524+9977C>A
ENST00000682052.1:n.1909+9977C>A
ENST00000682090.1:c.1524+9977C>A	ENSP00000508130.1:n.1524+9977C>A
ENST00000682115.1:c.1524+9977C>A	ENSP00000508069.1:n.1524+9977C>A
ENST00000682222.1:c.1524+9977C>A	ENSP00000506840.1:n.1524+9977C>A
ENST00000682716.1:n.1909+9977C>A
ENST00000682823.1:n.1910-9548C>A
ENST00000683208.1:c.1525-9548C>A	ENSP00000508151.1:n.1525-9548C>A
ENST00000683215.1:c.1524+9977C>A	ENSP00000507424.1:n.1524+9977C>A
ENST00000683774.1:n.2165+9977C>A
ENST00000683806.1:c.*1551+9977C>A	ENSP00000506783.1:n.*1551+9977C>A
ENST00000683903.1:c.1296+9977C>A	ENSP00000507071.1:n.1296+9977C>A
ENST00000684027.1:c.*327+9977C>A	ENSP00000508056.1:n.*327+9977C>A
ENST00000684068.1:c.1524+9977C>A	ENSP00000508175.1:n.1524+9977C>A
ENST00000684279.1:n.1909+9977C>A
ENST00000684518.1:c.*568+9977C>A	ENSP00000507289.1:n.*568+9977C>A
ENST00000369134.9:c.1524+9977C>A MANE Select	ENSP00000358130.6:n.1524+9977C>A
ENST00000369137.8:c.*1515+9977C>A	ENSP00000358133.5:n.*1515+9977C>A
ENST00000421544.6:c.1524+9977C>A	ENSP00000397026.1:n.1524+9977C>A
ENST00000318991.10:c.1410+9977C>A	ENSP00000313276.7:n.1410+9977C>A
ENST00000369134.8:c.1410+9977C>A	ENSP00000358130.5:n.1410+9977C>A
ENST00000369137.7:c.1410+9977C>A	ENSP00000358133.4:n.1410+9977C>A
ENST00000369138.5:c.1524+9977C>A	ENSP00000358134.1:n.1524+9977C>A
ENST00000413795.5:c.1524+9977C>A	ENSP00000405596.1:n.1524+9977C>A
ENST00000421544.5:c.1524+9977C>A	ENSP00000397026.1:n.1524+9977C>A
ENST00000436862.1:c.321+9977C>A	ENSP00000407140.1:n.321+9977C>A
NM_001166247.1:c.1524+9977C>A	NP_001159719.1:n.1524+9977C>A
NM_021956.4:c.1524+9977C>A	NP_068775.1:n.1524+9977C>A
NM_175768.3:c.1524+9977C>A	NP_786944.1:n.1524+9977C>A
XM_005266945.2:c.1524+9977C>A	XP_005267002.1:n.1524+9977C>A
XM_005266946.2:c.1377+9977C>A	XP_005267003.1:n.1377+9977C>A
XM_011535777.1:c.1524+9977C>A	XP_011534079.1:n.1524+9977C>A
XM_011535778.1:c.1524+9977C>A	XP_011534080.1:n.1524+9977C>A
XM_011535779.1:c.1524+9977C>A	XP_011534081.1:n.1524+9977C>A
XM_011535780.1:c.1524+9977C>A	XP_011534082.1:n.1524+9977C>A
XM_011535781.1:c.1524+9977C>A	XP_011534083.1:n.1524+9977C>A
XM_005266946.4:c.1377+9977C>A	XP_005267003.1:n.1377+9977C>A
XM_011535777.3:c.1524+9977C>A	XP_011534079.1:n.1524+9977C>A
XM_017010781.2:c.1524+9977C>A	XP_016866270.1:n.1524+9977C>A
XM_017010782.2:c.1524+9977C>A	XP_016866271.1:n.1524+9977C>A
XM_024446410.1:c.1524+9977C>A	XP_024302178.1:n.1524+9977C>A
XM_024446411.1:c.1524+9977C>A	XP_024302179.1:n.1524+9977C>A
XR_002956278.1:n.1947+9977C>A
NM_021956.5:c.1524+9977C>A MANE Select	NP_068775.1:n.1524+9977C>A