Canonical Allele Identifier: CA2339887542
Gene: GRIN2D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48419528_48419535delinsTCCCTTCC , CM000681.2:g.48419528_48419535delinsTCCCTTCC GRCh38
NC_000019.9:g.48922785_48922792delinsTCCCTTCC , CM000681.1:g.48922785_48922792delinsTCCCTTCC GRCh37
NC_000019.8:g.53614597_53614604delinsTCCCTTCC NCBI36
NG_052829.1:g.29654_29661delinsTCCCTTCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000263269.4:c.1862-57_1862-50delinsTCCCTTCC MANE Select ENSP00000263269.2:n.1862-57_1862-50delinsTCCCTTCC
ENST00000263269.3:c.1862-57_1862-50delinsTCCCTTCC ENSP00000263269.2:n.1862-57_1862-50delinsTCCCTTCC
NM_000836.2:c.1862-57_1862-50delinsTCCCTTCC NP_000827.2:n.1862-57_1862-50delinsTCCCTTCC
XM_011526872.1:c.1862-57_1862-50delinsTCCCTTCC XP_011525174.1:n.1862-57_1862-50delinsTCCCTTCC
NM_000836.4:c.1862-57_1862-50delinsTCCCTTCC MANE Select NP_000827.2:n.1862-57_1862-50delinsTCCCTTCC