Canonical Allele Identifier: CA1592403940
Gene: GRIA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.153599994C= , CM000667.2:g.153599994C= GRCh38
NC_000005.9:g.152979554C= , CM000667.1:g.152979554C= GRCh37
NC_000005.8:g.152959747C= NCBI36
NG_047078.1:g.115299C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000340592.10:c.221-46934C= ENSP00000339343.5:n.221-46934C=
ENST00000520353.6:c.14-46934C= ENSP00000516539.1:n.14-46934C=
ENST00000706733.1:c.221-46934C= ENSP00000516520.1:n.221-46934C=
ENST00000706734.1:c.248-46934C= ENSP00000516521.1:n.248-46934C=
ENST00000706767.1:c.83-46934C= ENSP00000516540.1:n.83-46934C=
ENST00000285900.10:c.221-46934C= MANE Select ENSP00000285900.4:n.221-46934C=
ENST00000285900.9:c.221-46934C= ENSP00000285900.4:n.221-46934C=
ENST00000340592.9:c.221-46934C= ENSP00000339343.5:n.221-46934C=
ENST00000448073.8:c.251-46934C= ENSP00000415569.2:n.251-46934C=
ENST00000481559.6:n.362-46934C=
ENST00000518142.5:c.221-50336C= ENSP00000427920.1:n.221-50336C=
ENST00000518783.1:c.251-46934C= ENSP00000428994.1:n.251-46934C=
ENST00000518862.5:n.169-46934C=
ENST00000520966.1:n.88+25603C=
ENST00000521843.6:c.14-46934C= ENSP00000427864.2:n.14-46934C=
NM_000827.3:c.221-46934C= NP_000818.2:n.221-46934C=
NM_001114183.1:c.221-46934C= NP_001107655.1:n.221-46934C=
NM_001258019.1:c.221-50336C= NP_001244948.1:n.221-50336C=
NM_001258020.1:c.-65-46934C= NP_001244949.1:n.-65-46934C=
NM_001258021.1:c.251-46934C= NP_001244950.1:n.251-46934C=
NM_001258022.1:c.251-46934C= NP_001244951.1:n.251-46934C=
NM_001258023.1:c.14-46934C= NP_001244952.1:n.14-46934C=
NR_047578.1:n.448-46934C=
XM_011537635.1:c.161-46934C= XP_011535937.1:n.161-46934C=
XR_427776.2:n.491-46934C=
NM_001364165.1:c.221-46934C= NP_001351094.1:n.221-46934C=
NM_001364166.1:c.248-46934C= NP_001351095.1:n.248-46934C=
NM_001364167.1:c.14-46934C= NP_001351096.1:n.14-46934C=
NR_157093.1:n.440-46934C=
XM_017009392.1:c.251-46934C= XP_016864881.1:n.251-46934C=
NM_000827.4:c.221-46934C= MANE Select NP_000818.2:n.221-46934C=
NM_001114183.2:c.221-46934C= NP_001107655.1:n.221-46934C=
NM_001258019.2:c.221-50336C= NP_001244948.1:n.221-50336C=
NM_001258020.2:c.-65-46934C= NP_001244949.1:n.-65-46934C=
NM_001258021.2:c.251-46934C= NP_001244950.1:n.251-46934C=
NM_001258022.2:c.251-46934C= NP_001244951.1:n.251-46934C=
NM_001364165.2:c.221-46934C= NP_001351094.1:n.221-46934C=
NM_001364166.2:c.248-46934C= NP_001351095.1:n.248-46934C=
NM_001364167.2:c.14-46934C= NP_001351096.1:n.14-46934C=
NR_047578.2:n.302-46934C=
NR_157093.2:n.440-46934C=