Canonical Allele Identifier: CA2838338318

Gene: GRIK2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.101707323C>T , CM000668.2:g.101707323C>T	GRCh38
NC_000006.11:g.102155198C>T , CM000668.1:g.102155198C>T	GRCh37
NC_000006.10:g.102261891C>T	NCBI36
NG_009224.2:g.313294C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436862.2:c.928+20993C>T	ENSP00000407140.2:n.928+20993C>T
ENST00000681975.1:c.951+20970C>T	ENSP00000508014.1:n.951+20970C>T
ENST00000682052.1:n.1336+20970C>T
ENST00000682090.1:c.951+20970C>T	ENSP00000508130.1:n.951+20970C>T
ENST00000682115.1:c.951+20970C>T	ENSP00000508069.1:n.951+20970C>T
ENST00000682222.1:c.951+20970C>T	ENSP00000506840.1:n.951+20970C>T
ENST00000682716.1:n.1336+20970C>T
ENST00000682823.1:n.1336+20970C>T
ENST00000683208.1:c.951+20970C>T	ENSP00000508151.1:n.951+20970C>T
ENST00000683215.1:c.951+20970C>T	ENSP00000507424.1:n.951+20970C>T
ENST00000683774.1:n.1592+20970C>T
ENST00000683806.1:c.*978+20970C>T	ENSP00000506783.1:n.*978+20970C>T
ENST00000683903.1:c.723+30519C>T	ENSP00000507071.1:n.723+30519C>T
ENST00000684027.1:c.951+20970C>T	ENSP00000508056.1:n.951+20970C>T
ENST00000684068.1:c.951+20970C>T	ENSP00000508175.1:n.951+20970C>T
ENST00000684279.1:n.1336+20970C>T
ENST00000684518.1:c.928+20993C>T	ENSP00000507289.1:n.928+20993C>T
ENST00000369134.9:c.951+20970C>T MANE Select	ENSP00000358130.6:n.951+20970C>T
ENST00000369137.8:c.*942+20970C>T	ENSP00000358133.5:n.*942+20970C>T
ENST00000421544.6:c.951+20970C>T	ENSP00000397026.1:n.951+20970C>T
ENST00000318991.10:c.837+20970C>T	ENSP00000313276.7:n.837+20970C>T
ENST00000358361.7:c.951+20970C>T	ENSP00000351128.3:n.951+20970C>T
ENST00000369134.8:c.837+20970C>T	ENSP00000358130.5:n.837+20970C>T
ENST00000369137.7:c.837+20970C>T	ENSP00000358133.4:n.837+20970C>T
ENST00000369138.5:c.951+20970C>T	ENSP00000358134.1:n.951+20970C>T
ENST00000413795.5:c.951+20970C>T	ENSP00000405596.1:n.951+20970C>T
ENST00000421544.5:c.951+20970C>T	ENSP00000397026.1:n.951+20970C>T
ENST00000455610.5:c.90+24717C>T	ENSP00000391988.1:n.90+24717C>T
NM_001166247.1:c.951+20970C>T	NP_001159719.1:n.951+20970C>T
NM_021956.4:c.951+20970C>T	NP_068775.1:n.951+20970C>T
NM_175768.3:c.951+20970C>T	NP_786944.1:n.951+20970C>T
XM_005266945.2:c.951+20970C>T	XP_005267002.1:n.951+20970C>T
XM_005266946.2:c.804+20970C>T	XP_005267003.1:n.804+20970C>T
XM_011535777.1:c.951+20970C>T	XP_011534079.1:n.951+20970C>T
XM_011535778.1:c.951+20970C>T	XP_011534080.1:n.951+20970C>T
XM_011535779.1:c.951+20970C>T	XP_011534081.1:n.951+20970C>T
XM_011535780.1:c.951+20970C>T	XP_011534082.1:n.951+20970C>T
XM_011535781.1:c.951+20970C>T	XP_011534083.1:n.951+20970C>T
XM_005266946.4:c.804+20970C>T	XP_005267003.1:n.804+20970C>T
XM_011535777.3:c.951+20970C>T	XP_011534079.1:n.951+20970C>T
XM_017010781.2:c.951+20970C>T	XP_016866270.1:n.951+20970C>T
XM_017010782.2:c.951+20970C>T	XP_016866271.1:n.951+20970C>T
XM_024446410.1:c.951+20970C>T	XP_024302178.1:n.951+20970C>T
XM_024446411.1:c.951+20970C>T	XP_024302179.1:n.951+20970C>T
XR_002956278.1:n.1374+20970C>T
NM_021956.5:c.951+20970C>T MANE Select	NP_068775.1:n.951+20970C>T