Canonical Allele Identifier: CA12039921

Gene: GRIA1

Linked Data

• dbSNP Id: rs6889909
• gnomAD v2: 5-153123433-C-T
• gnomAD v3: 5-153743873-C-T
• gnomAD v4: 5-153743873-C-T
• MyVariant Identifiers: chr5:g.153123433C>T (hg19) ; chr5:g.153743873C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.153743873C>T , CM000667.2:g.153743873C>T	GRCh38
NC_000005.9:g.153123433C>T , CM000667.1:g.153123433C>T	GRCh37
NC_000005.8:g.153103626C>T	NCBI36
NG_047078.1:g.259178C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000340592.10:c.1824-20561C>T	ENSP00000339343.5:n.1824-20561C>T
ENST00000706733.1:c.1824-20561C>T	ENSP00000516520.1:n.1824-20561C>T
ENST00000706734.1:c.1851-20561C>T	ENSP00000516521.1:n.1851-20561C>T
ENST00000285900.10:c.1824-20561C>T MANE Select	ENSP00000285900.4:n.1824-20561C>T
ENST00000285900.9:c.1824-20561C>T	ENSP00000285900.4:n.1824-20561C>T
ENST00000340592.9:c.1824-20561C>T	ENSP00000339343.5:n.1824-20561C>T
ENST00000448073.8:c.1854-20561C>T	ENSP00000415569.2:n.1854-20561C>T
ENST00000518142.5:c.1584-20561C>T	ENSP00000427920.1:n.1584-20561C>T
ENST00000518783.1:c.1854-20561C>T	ENSP00000428994.1:n.1854-20561C>T
ENST00000521843.6:c.1617-20561C>T	ENSP00000427864.2:n.1617-20561C>T
NM_000827.3:c.1824-20561C>T	NP_000818.2:n.1824-20561C>T
NM_001114183.1:c.1824-20561C>T	NP_001107655.1:n.1824-20561C>T
NM_001258019.1:c.1584-20561C>T	NP_001244948.1:n.1584-20561C>T
NM_001258020.1:c.1539-20561C>T	NP_001244949.1:n.1539-20561C>T
NM_001258021.1:c.1854-20561C>T	NP_001244950.1:n.1854-20561C>T
NM_001258022.1:c.1854-20561C>T	NP_001244951.1:n.1854-20561C>T
NM_001258023.1:c.1617-20561C>T	NP_001244952.1:n.1617-20561C>T
NR_047578.1:n.2051-20561C>T
XM_011537635.1:c.1764-20561C>T	XP_011535937.1:n.1764-20561C>T
XR_427776.2:n.2094-20561C>T
NM_001364165.1:c.1656-20561C>T	NP_001351094.1:n.1656-20561C>T
NM_001364166.1:c.1851-20561C>T	NP_001351095.1:n.1851-20561C>T
NM_001364167.1:c.1617-20561C>T	NP_001351096.1:n.1617-20561C>T
NR_157093.1:n.2043-20561C>T
XM_017009392.1:c.1854-20561C>T	XP_016864881.1:n.1854-20561C>T
NM_000827.4:c.1824-20561C>T MANE Select	NP_000818.2:n.1824-20561C>T
NM_001114183.2:c.1824-20561C>T	NP_001107655.1:n.1824-20561C>T
NM_001258019.2:c.1584-20561C>T	NP_001244948.1:n.1584-20561C>T
NM_001258020.2:c.1539-20561C>T	NP_001244949.1:n.1539-20561C>T
NM_001258021.2:c.1854-20561C>T	NP_001244950.1:n.1854-20561C>T
NM_001258022.2:c.1854-20561C>T	NP_001244951.1:n.1854-20561C>T
NM_001364165.2:c.1656-20561C>T	NP_001351094.1:n.1656-20561C>T
NM_001364166.2:c.1851-20561C>T	NP_001351095.1:n.1851-20561C>T
NM_001364167.2:c.1617-20561C>T	NP_001351096.1:n.1617-20561C>T
NR_047578.2:n.1905-20561C>T
NR_157093.2:n.2043-20561C>T