Canonical Allele Identifier: CA1868369266
Gene: GRIN3A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101615556_101615558delinsCCG , CM000671.2:g.101615556_101615558delinsCCG GRCh38
NC_000009.11:g.104377838_104377840delinsCCG , CM000671.1:g.104377838_104377840delinsCCG GRCh37
NC_000009.10:g.103417659_103417661delinsCCG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361820.6:c.2615-2031_2615-2029delinsCGG MANE Select ENSP00000355155.3:n.2615-2031_2615-2029delinsCGG
ENST00000361820.3:c.2615-2031_2615-2029delinsCGG ENSP00000355155.3:n.2615-2031_2615-2029delinsCGG
NM_133445.2:c.2615-2031_2615-2029delinsCGG NP_597702.2:n.2615-2031_2615-2029delinsCGG
XM_011518211.1:c.2615-2031_2615-2029delinsCGG XP_011516513.1:n.2615-2031_2615-2029delinsCGG
XM_011518212.1:c.2615-2031_2615-2029delinsCGG XP_011516514.1:n.2615-2031_2615-2029delinsCGG
XR_929711.1:n.2702-2031_2702-2029delinsCGG
XM_011518211.2:c.2615-2031_2615-2029delinsCGG XP_011516513.1:n.2615-2031_2615-2029delinsCGG
NM_133445.3:c.2615-2031_2615-2029delinsCGG MANE Select NP_597702.2:n.2615-2031_2615-2029delinsCGG