Canonical Allele Identifier: CA974532117

Gene: GRIN2A

Linked Data

• gnomAD v3: 16-9764196-C-CTCGT
• gnomAD v4: 16-9764196-C-CTCGT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9764197_9764198insCGTT , CM000678.2:g.9764197_9764198insCGTT	GRCh38
NC_000016.9:g.9858054_9858055insCGTT , CM000678.1:g.9858054_9858055insCGTT	GRCh37
NC_000016.8:g.9765555_9765556insCGTT	NCBI36
NG_011812.1:g.423558_423559insACGA
NG_011812.2:g.423558_423559insACGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.3347_3348insACGA MANE Select	ENSP00000332549.3:p.Ile1117ArgfsTer8
ENST00000535259.6:c.2876_2877insACGA	ENSP00000441572.3:p.Ile960ArgfsTer8
ENST00000636273.2:n.2940_2941insACGA
ENST00000674742.1:c.2876_2877insACGA	ENSP00000502200.1:p.Ile960ArgfsTer8
ENST00000675398.1:c.*717_*718insACGA	ENSP00000502752.1:n.*717_*718insACGA
ENST00000330684.3:c.3347_3348insACGA	ENSP00000332549.3:p.Ile1117ArgfsTer8
ENST00000396573.6:c.3347_3348insACGA	ENSP00000379818.2:p.Ile1117ArgfsTer8
ENST00000396575.6:c.2936_2937insACGA	ENSP00000379820.3:p.Ile980ArgfsTer8
ENST00000461292.3:n.2986_2987insACGA
ENST00000535259.5:c.2936_2937insACGA	ENSP00000441572.2:p.Ile980ArgfsTer8
ENST00000562109.5:c.3347_3348insACGA	ENSP00000454998.1:p.Ile1117ArgfsTer8
NM_000833.4:c.3347_3348insACGA	NP_000824.1:p.Ile1117ArgfsTer8
NM_001134407.2:c.3347_3348insACGA	NP_001127879.1:p.Ile1117ArgfsTer8
NM_001134408.2:c.3347_3348insACGA	NP_001127880.1:p.Ile1117ArgfsTer8
XM_011522456.1:c.3188_3189insACGA	XP_011520758.1:p.Ile1064ArgfsTer8
XM_011522457.1:c.3089_3090insACGA	XP_011520759.1:p.Ile1031ArgfsTer8
XM_011522458.1:c.2876_2877insACGA	XP_011520760.1:p.Ile960ArgfsTer8
XM_011522459.1:c.2876_2877insACGA	XP_011520761.1:p.Ile960ArgfsTer8
XM_011522460.1:c.2876_2877insACGA	XP_011520762.1:p.Ile960ArgfsTer8
XM_011522461.1:c.3347_3348insACGA	XP_011520763.1:p.Ile1117ArgfsTer8
XM_011522458.3:c.2876_2877insACGA	XP_011520760.1:p.Ile960ArgfsTer8
XM_011522461.3:c.3347_3348insACGA	XP_011520763.1:p.Ile1117ArgfsTer8
XM_017023172.1:c.3503_3504insACGA	XP_016878661.1:p.Ile1169ArgfsTer8
XM_017023173.1:c.3503_3504insACGA	XP_016878662.1:p.Ile1169ArgfsTer8
NM_001134407.3:c.3347_3348insACGA MANE Select	NP_001127879.1:p.Ile1117ArgfsTer8
NM_000833.5:c.3347_3348insACGA	NP_000824.1:p.Ile1117ArgfsTer8