Canonical Allele Identifier: CA2339887526

Gene: GRIN2D

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48419509_48419511delinsTTC , CM000681.2:g.48419509_48419511delinsTTC	GRCh38
NC_000019.9:g.48922766_48922768delinsTTC , CM000681.1:g.48922766_48922768delinsTTC	GRCh37
NC_000019.8:g.53614578_53614580delinsTTC	NCBI36
NG_052829.1:g.29635_29637delinsTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263269.4:c.1862-76_1862-74delinsTTC MANE Select	ENSP00000263269.2:n.1862-76_1862-74delinsTTC
ENST00000263269.3:c.1862-76_1862-74delinsTTC	ENSP00000263269.2:n.1862-76_1862-74delinsTTC
NM_000836.2:c.1862-76_1862-74delinsTTC	NP_000827.2:n.1862-76_1862-74delinsTTC
XM_011526872.1:c.1862-76_1862-74delinsTTC	XP_011525174.1:n.1862-76_1862-74delinsTTC
NM_000836.4:c.1862-76_1862-74delinsTTC MANE Select	NP_000827.2:n.1862-76_1862-74delinsTTC