Canonical Allele Identifier: CA12446521

Gene: GRIK2

Linked Data

• dbSNP Id: rs2518224
• gnomAD v2: 6-101906652-A-C
• gnomAD v3: 6-101458776-A-C
• gnomAD v4: 6-101458776-A-C
• MyVariant Identifiers: chr6:g.101906652A>C (hg19) ; chr6:g.101458776A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.101458776A>C , CM000668.2:g.101458776A>C	GRCh38
NC_000006.11:g.101906652A>C , CM000668.1:g.101906652A>C	GRCh37
NC_000006.10:g.102013370A>C	NCBI36
NG_009224.2:g.64748A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000436862.2:c.115+59384A>C	ENSP00000407140.2:n.115+59384A>C
ENST00000681975.1:c.115+59384A>C	ENSP00000508014.1:n.115+59384A>C
ENST00000682052.1:n.500+59384A>C
ENST00000682090.1:c.115+59384A>C	ENSP00000508130.1:n.115+59384A>C
ENST00000682115.1:c.115+59384A>C	ENSP00000508069.1:n.115+59384A>C
ENST00000682222.1:c.115+59384A>C	ENSP00000506840.1:n.115+59384A>C
ENST00000682716.1:n.500+59384A>C
ENST00000682823.1:n.500+59384A>C
ENST00000683208.1:c.115+59384A>C	ENSP00000508151.1:n.115+59384A>C
ENST00000683215.1:c.115+59384A>C	ENSP00000507424.1:n.115+59384A>C
ENST00000683747.1:n.500+59384A>C
ENST00000683774.1:n.756+59384A>C
ENST00000683806.1:c.115+59384A>C	ENSP00000506783.1:n.115+59384A>C
ENST00000683903.1:c.115+59384A>C	ENSP00000507071.1:n.115+59384A>C
ENST00000684027.1:c.115+59384A>C	ENSP00000508056.1:n.115+59384A>C
ENST00000684068.1:c.115+59384A>C	ENSP00000508175.1:n.115+59384A>C
ENST00000684279.1:n.500+59384A>C
ENST00000684518.1:c.115+59384A>C	ENSP00000507289.1:n.115+59384A>C
ENST00000369134.9:c.115+59384A>C MANE Select	ENSP00000358130.6:n.115+59384A>C
ENST00000369137.8:c.116-37191A>C	ENSP00000358133.5:n.116-37191A>C
ENST00000421544.6:c.115+59384A>C	ENSP00000397026.1:n.115+59384A>C
ENST00000358361.7:c.115+59384A>C	ENSP00000351128.3:n.115+59384A>C
ENST00000369138.5:c.115+59384A>C	ENSP00000358134.1:n.115+59384A>C
ENST00000413795.5:c.115+59384A>C	ENSP00000405596.1:n.115+59384A>C
ENST00000421544.5:c.115+59384A>C	ENSP00000397026.1:n.115+59384A>C
NM_001166247.1:c.115+59384A>C	NP_001159719.1:n.115+59384A>C
NM_021956.4:c.115+59384A>C	NP_068775.1:n.115+59384A>C
NM_175768.3:c.115+59384A>C	NP_786944.1:n.115+59384A>C
XM_005266945.2:c.115+59384A>C	XP_005267002.1:n.115+59384A>C
XM_011535777.1:c.115+59384A>C	XP_011534079.1:n.115+59384A>C
XM_011535778.1:c.115+59384A>C	XP_011534080.1:n.115+59384A>C
XM_011535779.1:c.115+59384A>C	XP_011534081.1:n.115+59384A>C
XM_011535780.1:c.115+59384A>C	XP_011534082.1:n.115+59384A>C
XM_011535781.1:c.115+59384A>C	XP_011534083.1:n.115+59384A>C
XR_942819.1:n.249+917A>C
XM_011535777.3:c.115+59384A>C	XP_011534079.1:n.115+59384A>C
XM_017010781.2:c.115+59384A>C	XP_016866270.1:n.115+59384A>C
XM_017010782.2:c.115+59384A>C	XP_016866271.1:n.115+59384A>C
XM_024446410.1:c.115+59384A>C	XP_024302178.1:n.115+59384A>C
XM_024446411.1:c.115+59384A>C	XP_024302179.1:n.115+59384A>C
XR_002956278.1:n.538+59384A>C
NM_021956.5:c.115+59384A>C MANE Select	NP_068775.1:n.115+59384A>C