Canonical Allele Identifier: CA374271703
Gene: GRIN3A HGNC NCBI

Linked Data

COSMIC: COSM4520707
MyVariant Identifiers: chr9:g.104449112C>T (hg19) chr9:g.101686830C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101686830C>T , CM000671.2:g.101686830C>T GRCh38
NC_000009.11:g.104449112C>T , CM000671.1:g.104449112C>T GRCh37
NC_000009.10:g.103488933C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361820.6:c.1070G>A MANE Select ENSP00000355155.3:p.Gly357Glu
ENST00000361820.3:c.1070G>A ENSP00000355155.3:p.Gly357Glu
NM_133445.2:c.1070G>A NP_597702.2:p.Gly357Glu
XM_011518211.1:c.1070G>A XP_011516513.1:p.Gly357Glu
XM_011518212.1:c.1070G>A XP_011516514.1:p.Gly357Glu
XR_929711.1:n.1157G>A
XM_011518211.2:c.1070G>A XP_011516513.1:p.Gly357Glu
NM_133445.3:c.1070G>A MANE Select NP_597702.2:p.Gly357Glu
Search 100 bp 5'
Search 100 bp 3'