Canonical Allele Identifier: CA1868369381
Gene: GRIN3A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101615636T= , CM000671.2:g.101615636T= GRCh38
NC_000009.11:g.104377918T= , CM000671.1:g.104377918T= GRCh37
NC_000009.10:g.103417739T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000361820.6:c.2615-2109A= MANE Select ENSP00000355155.3:n.2615-2109A=
ENST00000361820.3:c.2615-2109A= ENSP00000355155.3:n.2615-2109A=
NM_133445.2:c.2615-2109A= NP_597702.2:n.2615-2109A=
XM_011518211.1:c.2615-2109A= XP_011516513.1:n.2615-2109A=
XM_011518212.1:c.2615-2109A= XP_011516514.1:n.2615-2109A=
XR_929711.1:n.2702-2109A=
XM_011518211.2:c.2615-2109A= XP_011516513.1:n.2615-2109A=
NM_133445.3:c.2615-2109A= MANE Select NP_597702.2:n.2615-2109A=