Canonical Allele Identifier: CA805893244

Gene: GRIA1

Linked Data

• dbSNP Id: rs1422222214
• MyVariant Identifiers: chr5:g.152940124del (hg19) ; chr5:g.153560564del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.153560566del , CM000667.2:g.153560566del	GRCh38
NC_000005.9:g.152940126del , CM000667.1:g.152940126del	GRCh37
NC_000005.8:g.152920319del	NCBI36
NG_047078.1:g.75871del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340592.10:c.220+66501del	ENSP00000339343.5:n.220+66501del
ENST00000520353.6:c.13+66501del	ENSP00000516539.1:n.13+66501del
ENST00000706733.1:c.220+66501del	ENSP00000516520.1:n.220+66501del
ENST00000706734.1:c.247+66501del	ENSP00000516521.1:n.247+66501del
ENST00000706767.1:c.82+69596del	ENSP00000516540.1:n.82+69596del
ENST00000285900.10:c.220+66501del MANE Select	ENSP00000285900.4:n.220+66501del
ENST00000285900.9:c.220+66501del	ENSP00000285900.4:n.220+66501del
ENST00000340592.9:c.220+66501del	ENSP00000339343.5:n.220+66501del
ENST00000448073.8:c.250+66501del	ENSP00000415569.2:n.250+66501del
ENST00000481559.6:n.361+66501del
ENST00000518142.5:c.220+66501del	ENSP00000427920.1:n.220+66501del
ENST00000518783.1:c.250+66501del	ENSP00000428994.1:n.250+66501del
ENST00000518862.5:n.168+66501del
ENST00000521843.6:c.13+66501del	ENSP00000427864.2:n.13+66501del
NM_000827.3:c.220+66501del	NP_000818.2:n.220+66501del
NM_001114183.1:c.220+66501del	NP_001107655.1:n.220+66501del
NM_001258019.1:c.220+66501del	NP_001244948.1:n.220+66501del
NM_001258020.1:c.-66+50760del	NP_001244949.1:n.-66+50760del
NM_001258021.1:c.250+66501del	NP_001244950.1:n.250+66501del
NM_001258022.1:c.250+66501del	NP_001244951.1:n.250+66501del
NM_001258023.1:c.13+66501del	NP_001244952.1:n.13+66501del
NR_047578.1:n.447+69596del
XM_011537635.1:c.160+66501del	XP_011535937.1:n.160+66501del
XR_427776.2:n.490+66501del
NM_001364165.1:c.220+66501del	NP_001351094.1:n.220+66501del
NM_001364166.1:c.247+66501del	NP_001351095.1:n.247+66501del
NM_001364167.1:c.13+66501del	NP_001351096.1:n.13+66501del
NR_157093.1:n.439+66501del
XM_017009392.1:c.250+66501del	XP_016864881.1:n.250+66501del
NM_000827.4:c.220+66501del MANE Select	NP_000818.2:n.220+66501del
NM_001114183.2:c.220+66501del	NP_001107655.1:n.220+66501del
NM_001258019.2:c.220+66501del	NP_001244948.1:n.220+66501del
NM_001258020.2:c.-66+50760del	NP_001244949.1:n.-66+50760del
NM_001258021.2:c.250+66501del	NP_001244950.1:n.250+66501del
NM_001258022.2:c.250+66501del	NP_001244951.1:n.250+66501del
NM_001364165.2:c.220+66501del	NP_001351094.1:n.220+66501del
NM_001364166.2:c.247+66501del	NP_001351095.1:n.247+66501del
NM_001364167.2:c.13+66501del	NP_001351096.1:n.13+66501del
NR_047578.2:n.301+69596del
NR_157093.2:n.439+66501del