Canonical Allele Identifier: CA375730083

Gene: GRIN1

Linked Data

• gnomAD v4: 9-137167513-C-T
• MyVariant Identifiers: chr9:g.140061965C>T (hg19) ; chr9:g.137167513C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137167513C>T , CM000671.2:g.137167513C>T	GRCh38
NC_000009.11:g.140061965C>T , CM000671.1:g.140061965C>T	GRCh37
NC_000009.10:g.139181786C>T	NCBI36
NG_011507.1:g.33357C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371553.8:c.2764-261C>T	ENSP00000360608.3:n.2764-261C>T
ENST00000371560.5:c.2653-261C>T	ENSP00000360615.3:n.2653-261C>T
ENST00000371561.8:c.2803C>T MANE Select	ENSP00000360616.3:p.His935Tyr
ENST00000371546.8:c.2866C>T	ENSP00000360601.4:p.His956Tyr
ENST00000371550.8:c.2692C>T	ENSP00000360605.4:p.His898Tyr
ENST00000371553.7:c.2764-261C>T	ENSP00000360608.3:n.2764-261C>T
ENST00000371555.8:c.2755C>T	ENSP00000360610.4:p.His919Tyr
ENST00000371559.8:c.2590-261C>T	ENSP00000360614.4:n.2590-261C>T
ENST00000371560.4:c.2653-261C>T	ENSP00000360615.3:n.2653-261C>T
ENST00000371561.7:c.2803C>T	ENSP00000360616.3:p.His935Tyr
ENST00000473811.1:n.283C>T
NM_000832.6:c.2590-261C>T	NP_000823.4:n.2590-261C>T
NM_001185090.1:c.2764-261C>T	NP_001172019.1:n.2764-261C>T
NM_001185091.1:c.2653-261C>T	NP_001172020.1:n.2653-261C>T
NM_007327.3:c.2803C>T	NP_015566.1:p.His935Tyr
NM_021569.3:c.2692C>T	NP_067544.1:p.His898Tyr
XM_005266071.2:c.2701-261C>T	XP_005266128.1:n.2701-261C>T
XM_005266072.2:c.2755C>T	XP_005266129.1:p.His919Tyr
XM_005266073.3:c.2866C>T	XP_005266130.1:p.His956Tyr
XM_005266071.3:c.2701-261C>T	XP_005266128.1:n.2701-261C>T
XM_005266072.3:c.2755C>T	XP_005266129.1:p.His919Tyr
XM_005266073.4:c.2866C>T	XP_005266130.1:p.His956Tyr
NM_007327.4:c.2803C>T MANE Select	NP_015566.1:p.His935Tyr
NM_000832.7:c.2590-261C>T	NP_000823.4:n.2590-261C>T
NM_001185090.2:c.2764-261C>T	NP_001172019.1:n.2764-261C>T
NM_001185091.2:c.2653-261C>T	NP_001172020.1:n.2653-261C>T
NM_021569.4:c.2692C>T	NP_067544.1:p.His898Tyr