Canonical Allele Identifier: CA2631681582

Gene: GRIN2A

Linked Data

• gnomAD v4: 16-10179979-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10179980dup , CM000678.2:g.10179980dup	GRCh38
NC_000016.9:g.10273837dup , CM000678.1:g.10273837dup	GRCh37
NC_000016.8:g.10181338dup	NCBI36
NG_011812.1:g.7775dup
NG_011812.2:g.7775dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.414+18dup MANE Select	ENSP00000332549.3:n.414+18dup
ENST00000637334.1:n.93+18dup
ENST00000637393.1:c.6+18dup	ENSP00000490232.1:n.6+18dup
ENST00000675189.1:n.898+18dup
ENST00000675398.1:c.414+18dup	ENSP00000502752.1:n.414+18dup
ENST00000676032.1:n.865dup
ENST00000330684.3:c.414+18dup	ENSP00000332549.3:n.414+18dup
ENST00000396573.6:c.414+18dup	ENSP00000379818.2:n.414+18dup
ENST00000562109.5:c.414+18dup	ENSP00000454998.1:n.414+18dup
ENST00000566665.1:n.833dup
NM_000833.4:c.414+18dup	NP_000824.1:n.414+18dup
NM_001134407.2:c.414+18dup	NP_001127879.1:n.414+18dup
NM_001134408.2:c.414+18dup	NP_001127880.1:n.414+18dup
XM_011522461.1:c.414+18dup	XP_011520763.1:n.414+18dup
XM_011522461.3:c.414+18dup	XP_011520763.1:n.414+18dup
XM_017023172.1:c.570+18dup	XP_016878661.1:n.570+18dup
XM_017023173.1:c.570+18dup	XP_016878662.1:n.570+18dup
NM_001134407.3:c.414+18dup MANE Select	NP_001127879.1:n.414+18dup
NM_000833.5:c.414+18dup	NP_000824.1:n.414+18dup