Canonical Allele Identifier: CA3190138145

Gene: GRIA4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.105769711_105769712insAATT , CM000673.2:g.105769711_105769712insAATT	GRCh38
NC_000011.9:g.105640437_105640438insAATT , CM000673.1:g.105640437_105640438insAATT	GRCh37
NC_000011.8:g.105145647_105145648insAATT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_000829.4:c.487+16491_487+16492insAATT MANE Select	NP_000820.4:n.487+16491_487+16492insAATT
ENST00000282499.10:c.487+16491_487+16492insAATT MANE Select	ENSP00000282499.5:n.487+16491_487+16492insAATT
NM_000829.3:c.487+16491_487+16492insAATT	NP_000820.3:n.487+16491_487+16492insAATT
NM_001077243.2:c.487+16491_487+16492insAATT	NP_001070711.2:n.487+16491_487+16492insAATT
NM_001077243.3:c.487+16491_487+16492insAATT	NP_001070711.3:n.487+16491_487+16492insAATT
NM_001077244.1:c.487+16491_487+16492insAATT	NP_001070712.1:n.487+16491_487+16492insAATT
NM_001077244.2:c.487+16491_487+16492insAATT	NP_001070712.1:n.487+16491_487+16492insAATT
NM_001112812.1:c.487+16491_487+16492insAATT	NP_001106283.1:n.487+16491_487+16492insAATT
NM_001112812.2:c.487+16491_487+16492insAATT	NP_001106283.1:n.487+16491_487+16492insAATT
NR_046356.1:n.801+16491_801+16492insAATT
NR_046356.2:n.779+16491_779+16492insAATT
ENST00000282499.9:c.487+16491_487+16492insAATT	ENSP00000282499.5:n.487+16491_487+16492insAATT
ENST00000393125.6:c.487+16491_487+16492insAATT	ENSP00000376833.2:n.487+16491_487+16492insAATT
ENST00000393127.6:c.487+16491_487+16492insAATT	ENSP00000376835.2:n.487+16491_487+16492insAATT
ENST00000428631.6:c.487+16491_487+16492insAATT	ENSP00000415551.2:n.487+16491_487+16492insAATT
ENST00000525032.1:n.813+16491_813+16492insAATT
ENST00000525187.5:c.487+16491_487+16492insAATT	ENSP00000432180.1:n.487+16491_487+16492insAATT
ENST00000525187.6:c.487+16491_487+16492insAATT	ENSP00000432180.1:n.487+16491_487+16492insAATT
ENST00000530497.1:c.487+16491_487+16492insAATT	ENSP00000435775.1:n.487+16491_487+16492insAATT
ENST00000531011.5:c.487+16491_487+16492insAATT	ENSP00000432443.1:n.487+16491_487+16492insAATT
ENST00000703743.2:c.487+16491_487+16492insAATT	ENSP00000515457.2:n.487+16491_487+16492insAATT
ENST00000706777.1:c.487+16491_487+16492insAATT	ENSP00000516542.1:n.487+16491_487+16492insAATT
XM_005271518.2:c.487+16491_487+16492insAATT	XP_005271575.1:n.487+16491_487+16492insAATT
XM_005271518.3:c.487+16491_487+16492insAATT	XP_005271575.1:n.487+16491_487+16492insAATT
XM_006718823.1:c.487+16491_487+16492insAATT	XP_006718886.1:n.487+16491_487+16492insAATT
XM_006718823.2:c.487+16491_487+16492insAATT	XP_006718886.1:n.487+16491_487+16492insAATT
XM_011542775.1:c.487+16491_487+16492insAATT	XP_011541077.1:n.487+16491_487+16492insAATT
XM_011542775.2:c.487+16491_487+16492insAATT	XP_011541077.1:n.487+16491_487+16492insAATT
XM_017017609.1:c.487+16491_487+16492insAATT	XP_016873098.1:n.487+16491_487+16492insAATT
XM_017017610.2:c.487+16491_487+16492insAATT	XP_016873099.1:n.487+16491_487+16492insAATT
XM_024448454.1:c.487+16491_487+16492insAATT	XP_024304222.1:n.487+16491_487+16492insAATT
XM_024448455.1:c.487+16491_487+16492insAATT	XP_024304223.1:n.487+16491_487+16492insAATT
XR_001747841.1:n.977+16491_977+16492insAATT
XR_947825.1:n.977+16491_977+16492insAATT