Canonical Allele Identifier: CA2586189550

Gene: GRIN2D

Linked Data

• gnomAD v4: 19-48419519-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48419519_48419520insA , CM000681.2:g.48419519_48419520insA	GRCh38
NC_000019.9:g.48922776_48922777insA , CM000681.1:g.48922776_48922777insA	GRCh37
NC_000019.8:g.53614588_53614589insA	NCBI36
NG_052829.1:g.29645_29646insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263269.4:c.1862-66_1862-65insA MANE Select	ENSP00000263269.2:n.1862-66_1862-65insA
ENST00000263269.3:c.1862-66_1862-65insA	ENSP00000263269.2:n.1862-66_1862-65insA
NM_000836.2:c.1862-66_1862-65insA	NP_000827.2:n.1862-66_1862-65insA
XM_011526872.1:c.1862-66_1862-65insA	XP_011525174.1:n.1862-66_1862-65insA
NM_000836.4:c.1862-66_1862-65insA MANE Select	NP_000827.2:n.1862-66_1862-65insA