Canonical Allele Identifier: CA653205657
Gene: GRIN3A HGNC NCBI

Linked Data

COSMIC: COSN22578913
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101615675C>G , CM000671.2:g.101615675C>G GRCh38
NC_000009.11:g.104377957C>G , CM000671.1:g.104377957C>G GRCh37
NC_000009.10:g.103417778C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000361820.6:c.2615-2148G>C MANE Select ENSP00000355155.3:n.2615-2148G>C
ENST00000361820.3:c.2615-2148G>C ENSP00000355155.3:n.2615-2148G>C
NM_133445.2:c.2615-2148G>C NP_597702.2:n.2615-2148G>C
XM_011518211.1:c.2615-2148G>C XP_011516513.1:n.2615-2148G>C
XM_011518212.1:c.2615-2148G>C XP_011516514.1:n.2615-2148G>C
XR_929711.1:n.2702-2148G>C
XM_011518211.2:c.2615-2148G>C XP_011516513.1:n.2615-2148G>C
NM_133445.3:c.2615-2148G>C MANE Select NP_597702.2:n.2615-2148G>C
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