Canonical Allele Identifier: CA2814655032

Gene: GRIN2D

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48419537_48419538insTTTT , CM000681.2:g.48419537_48419538insTTTT	GRCh38
NC_000019.9:g.48922794_48922795insTTTT , CM000681.1:g.48922794_48922795insTTTT	GRCh37
NC_000019.8:g.53614606_53614607insTTTT	NCBI36
NG_052829.1:g.29663_29664insTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263269.4:c.1862-48_1862-47insTTTT MANE Select	ENSP00000263269.2:n.1862-48_1862-47insTTTT
ENST00000263269.3:c.1862-48_1862-47insTTTT	ENSP00000263269.2:n.1862-48_1862-47insTTTT
NM_000836.2:c.1862-48_1862-47insTTTT	NP_000827.2:n.1862-48_1862-47insTTTT
XM_011526872.1:c.1862-48_1862-47insTTTT	XP_011525174.1:n.1862-48_1862-47insTTTT
NM_000836.4:c.1862-48_1862-47insTTTT MANE Select	NP_000827.2:n.1862-48_1862-47insTTTT