Canonical Allele Identifier: CA974532246

Gene: GRIN2A

Linked Data

• gnomAD v3: 16-9764203-CTAG-C
• gnomAD v4: 16-9764203-CTAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9764204_9764206del , CM000678.2:g.9764204_9764206del	GRCh38
NC_000016.9:g.9858061_9858063del , CM000678.1:g.9858061_9858063del	GRCh37
NC_000016.8:g.9765562_9765564del	NCBI36
NG_011812.1:g.423549_423551del
NG_011812.2:g.423549_423551del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.3338_3340del MANE Select	ENSP00000332549.3:p.Pro1113del
ENST00000535259.6:c.2867_2869del	ENSP00000441572.3:p.Pro956del
ENST00000636273.2:n.2931_2933del
ENST00000674742.1:c.2867_2869del	ENSP00000502200.1:p.Pro956del
ENST00000675398.1:c.*708_*710del	ENSP00000502752.1:n.*708_*710del
ENST00000330684.3:c.3338_3340del	ENSP00000332549.3:p.Pro1113del
ENST00000396573.6:c.3338_3340del	ENSP00000379818.2:p.Pro1113del
ENST00000396575.6:c.2927_2929del	ENSP00000379820.3:p.Pro976del
ENST00000461292.3:n.2977_2979del
ENST00000535259.5:c.2927_2929del	ENSP00000441572.2:p.Pro976del
ENST00000562109.5:c.3338_3340del	ENSP00000454998.1:p.Pro1113del
NM_000833.4:c.3338_3340del	NP_000824.1:p.Pro1113del
NM_001134407.2:c.3338_3340del	NP_001127879.1:p.Pro1113del
NM_001134408.2:c.3338_3340del	NP_001127880.1:p.Pro1113del
XM_011522456.1:c.3179_3181del	XP_011520758.1:p.Pro1060del
XM_011522457.1:c.3080_3082del	XP_011520759.1:p.Pro1027del
XM_011522458.1:c.2867_2869del	XP_011520760.1:p.Pro956del
XM_011522459.1:c.2867_2869del	XP_011520761.1:p.Pro956del
XM_011522460.1:c.2867_2869del	XP_011520762.1:p.Pro956del
XM_011522461.1:c.3338_3340del	XP_011520763.1:p.Pro1113del
XM_011522458.3:c.2867_2869del	XP_011520760.1:p.Pro956del
XM_011522461.3:c.3338_3340del	XP_011520763.1:p.Pro1113del
XM_017023172.1:c.3494_3496del	XP_016878661.1:p.Pro1165del
XM_017023173.1:c.3494_3496del	XP_016878662.1:p.Pro1165del
NM_001134407.3:c.3338_3340del MANE Select	NP_001127879.1:p.Pro1113del
NM_000833.5:c.3338_3340del	NP_000824.1:p.Pro1113del