Canonical Allele Identifier: CA2206782595

Gene: GRIN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9938028_9938030delinsATG , CM000678.2:g.9938028_9938030delinsATG	GRCh38
NC_000016.9:g.10031885_10031887delinsATG , CM000678.1:g.10031885_10031887delinsATG	GRCh37
NC_000016.8:g.9939386_9939388delinsATG	NCBI36
NG_011812.1:g.249725_249727delinsCAT
NG_011812.2:g.249725_249727delinsCAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.936_938delinsCAT MANE Select	ENSP00000332549.3:p.Tyr312=
ENST00000535259.6:c.465_467delinsCAT	ENSP00000441572.3:p.Tyr155=
ENST00000636273.2:n.529_531delinsCAT
ENST00000637393.1:c.528_530delinsCAT	ENSP00000490232.1:p.Tyr176=
ENST00000674742.1:c.465_467delinsCAT	ENSP00000502200.1:p.Tyr155=
ENST00000675189.1:n.1420_1422delinsCAT
ENST00000675398.1:c.936_938delinsCAT	ENSP00000502752.1:p.Tyr312=
ENST00000330684.3:c.936_938delinsCAT	ENSP00000332549.3:p.Tyr312=
ENST00000396573.6:c.936_938delinsCAT	ENSP00000379818.2:p.Tyr312=
ENST00000396575.6:c.525_527delinsCAT	ENSP00000379820.3:p.Tyr175=
ENST00000461292.3:n.575_577delinsCAT
ENST00000535259.5:c.525_527delinsCAT	ENSP00000441572.2:p.Tyr175=
ENST00000562109.5:c.936_938delinsCAT	ENSP00000454998.1:p.Tyr312=
ENST00000566683.1:n.241-46930_241-46928delinsCAT
ENST00000568247.3:n.828_830delinsCAT
NM_000833.4:c.936_938delinsCAT	NP_000824.1:p.Tyr312=
NM_001134407.2:c.936_938delinsCAT	NP_001127879.1:p.Tyr312=
NM_001134408.2:c.936_938delinsCAT	NP_001127880.1:p.Tyr312=
XM_011522456.1:c.777_779delinsCAT	XP_011520758.1:p.Tyr259=
XM_011522457.1:c.678_680delinsCAT	XP_011520759.1:p.Tyr226=
XM_011522458.1:c.465_467delinsCAT	XP_011520760.1:p.Tyr155=
XM_011522459.1:c.465_467delinsCAT	XP_011520761.1:p.Tyr155=
XM_011522460.1:c.465_467delinsCAT	XP_011520762.1:p.Tyr155=
XM_011522461.1:c.936_938delinsCAT	XP_011520763.1:p.Tyr312=
XM_011522458.3:c.465_467delinsCAT	XP_011520760.1:p.Tyr155=
XM_011522461.3:c.936_938delinsCAT	XP_011520763.1:p.Tyr312=
XM_017023172.1:c.1092_1094delinsCAT	XP_016878661.1:p.Tyr364=
XM_017023173.1:c.1092_1094delinsCAT	XP_016878662.1:p.Tyr364=
NM_001134407.3:c.936_938delinsCAT MANE Select	NP_001127879.1:p.Tyr312=
NM_000833.5:c.936_938delinsCAT	NP_000824.1:p.Tyr312=