Canonical Allele Identifier: CA372541871
Gene: GRINA HGNC NCBI
PARP10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.143991438G>A , CM000670.2:g.143991438G>A GRCh38
NC_000008.10:g.145065606G>A , CM000670.1:g.145065606G>A GRCh37
NC_000008.9:g.145137594G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000395068.9:c.215G>A (GRINA) MANE Select ENSP00000378507.4:p.Gly72Asp
ENST00000313269.5:c.215G>A (GRINA) ENSP00000314380.5:p.Gly72Asp
ENST00000395068.8:c.215G>A (GRINA) ENSP00000378507.4:p.Gly72Asp
ENST00000529301.5:c.215G>A (GRINA) ENSP00000432706.1:p.Gly72Asp
ENST00000530478.5:c.-79-5000C>T (PARP10) ENSP00000436333.1:n.-79-5000C>T
ENST00000530898.1:c.215G>A (GRINA) ENSP00000436807.1:p.Gly72Asp
ENST00000531992.1:n.145G>A (GRINA)
NM_000837.1:c.215G>A (GRINA) NP_000828.1:p.Gly72Asp
NM_001009184.1:c.215G>A (GRINA) NP_001009184.1:p.Gly72Asp
XM_005250899.2:c.215G>A (GRINA) XP_005250956.1:p.Gly72Asp
NM_001009184.2:c.215G>A (GRINA) MANE Select NP_001009184.1:p.Gly72Asp
NM_000837.2:c.215G>A (GRINA) NP_000828.1:p.Gly72Asp