Canonical Allele Identifier: CA374271266
Gene: GRIN3A HGNC NCBI

Linked Data

gnomAD v4: 9-101686717-G-C
MyVariant Identifiers: chr9:g.104448999G>C (hg19) chr9:g.101686717G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101686717G>C , CM000671.2:g.101686717G>C GRCh38
NC_000009.11:g.104448999G>C , CM000671.1:g.104448999G>C GRCh37
NC_000009.10:g.103488820G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000361820.6:c.1183C>G MANE Select ENSP00000355155.3:p.Leu395Val
ENST00000361820.3:c.1183C>G ENSP00000355155.3:p.Leu395Val
NM_133445.2:c.1183C>G NP_597702.2:p.Leu395Val
XM_011518211.1:c.1183C>G XP_011516513.1:p.Leu395Val
XM_011518212.1:c.1183C>G XP_011516514.1:p.Leu395Val
XR_929711.1:n.1270C>G
XM_011518211.2:c.1183C>G XP_011516513.1:p.Leu395Val
NM_133445.3:c.1183C>G MANE Select NP_597702.2:p.Leu395Val
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