Canonical Allele Identifier: CA2529172488

Gene: GRIA3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.123428082del , CM000685.2:g.123428082del	GRCh38
NC_000023.10:g.122561933del , CM000685.1:g.122561933del	GRCh37
NC_000023.9:g.122389614del	NCBI36
NG_009377.2:g.248840del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000620443.2:c.2019del MANE Select	ENSP00000478489.1:p.Lys673AsnfsTer?
ENST00000622768.5:c.2019del MANE Plus Clinical	ENSP00000481554.1:p.Lys673AsnfsTer?
ENST00000541091.5:c.2019del	ENSP00000446440.2:p.Lys673AsnfsTer?
ENST00000620443.1:c.2019del	ENSP00000478489.1:p.Lys673AsnfsTer?
ENST00000620581.4:c.2019del	ENSP00000481875.1:p.Lys673AsnfsTer?
ENST00000622768.4:c.2019del	ENSP00000481554.1:p.Lys673AsnfsTer?
NM_000828.4:c.2019del	NP_000819.3:p.Lys673AsnfsTer?
NM_007325.4:c.2019del	NP_015564.4:p.Lys673AsnfsTer?
XR_938574.1:n.5217+9170del
NM_007325.5:c.2019del MANE Select	NP_015564.5:p.Lys673AsnfsTer?
NM_000828.5:c.2019del MANE Plus Clinical	NP_000819.4:p.Lys673AsnfsTer?