Canonical Allele Identifier: CA1884333319
Gene: GRIN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137167411A= , CM000671.2:g.137167411A= GRCh38
NC_000009.11:g.140061863A= , CM000671.1:g.140061863A= GRCh37
NC_000009.10:g.139181684A= NCBI36
NG_011507.1:g.33255A=

Transcript Alleles

HGVS Amino-acid change
ENST00000371553.8:c.2764-363A= ENSP00000360608.3:n.2764-363A=
ENST00000371560.5:c.2653-363A= ENSP00000360615.3:n.2653-363A=
ENST00000371561.8:c.2701A= MANE Select ENSP00000360616.3:p.Ser901=
ENST00000371546.8:c.2764A= ENSP00000360601.4:p.Ser922=
ENST00000371550.8:c.2590A= ENSP00000360605.4:p.Ser864=
ENST00000371553.7:c.2764-363A= ENSP00000360608.3:n.2764-363A=
ENST00000371555.8:c.2653A= ENSP00000360610.4:p.Ser885=
ENST00000371559.8:c.2590-363A= ENSP00000360614.4:n.2590-363A=
ENST00000371560.4:c.2653-363A= ENSP00000360615.3:n.2653-363A=
ENST00000371561.7:c.2701A= ENSP00000360616.3:p.Ser901=
ENST00000473811.1:n.181A=
NM_000832.6:c.2590-363A= NP_000823.4:n.2590-363A=
NM_001185090.1:c.2764-363A= NP_001172019.1:n.2764-363A=
NM_001185091.1:c.2653-363A= NP_001172020.1:n.2653-363A=
NM_007327.3:c.2701A= NP_015566.1:p.Ser901=
NM_021569.3:c.2590A= NP_067544.1:p.Ser864=
XM_005266071.2:c.2701-363A= XP_005266128.1:n.2701-363A=
XM_005266072.2:c.2653A= XP_005266129.1:p.Ser885=
XM_005266073.3:c.2764A= XP_005266130.1:p.Ser922=
XM_005266071.3:c.2701-363A= XP_005266128.1:n.2701-363A=
XM_005266072.3:c.2653A= XP_005266129.1:p.Ser885=
XM_005266073.4:c.2764A= XP_005266130.1:p.Ser922=
NM_007327.4:c.2701A= MANE Select NP_015566.1:p.Ser901=
NM_000832.7:c.2590-363A= NP_000823.4:n.2590-363A=
NM_001185090.2:c.2764-363A= NP_001172019.1:n.2764-363A=
NM_001185091.2:c.2653-363A= NP_001172020.1:n.2653-363A=
NM_021569.4:c.2590A= NP_067544.1:p.Ser864=