Canonical Allele Identifier: CA2336742746

Gene: GRIK5

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.42016956T= , CM000681.2:g.42016956T=	GRCh38
NC_000019.9:g.42521108T= , CM000681.1:g.42521108T=	GRCh37
NC_000019.8:g.47212948T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_002088.5:c.1871+4345A= MANE Select	NP_002079.3:n.1871+4345A=
ENST00000593562.6:c.1871+4345A= MANE Select	ENSP00000470251.1:n.1871+4345A=
NM_001301030.1:c.1871+4345A=	NP_001287959.1:n.1871+4345A=
NM_001301030.2:c.1871+4345A=	NP_001287959.1:n.1871+4345A=
NM_002088.4:c.1871+4345A=	NP_002079.3:n.1871+4345A=
ENST00000262895.7:c.1871+4345A=	ENSP00000262895.2:n.1871+4345A=
ENST00000301218.8:c.1871+4345A=	ENSP00000301218.3:n.1871+4345A=
ENST00000454993.6:n.748+4345A=
ENST00000593562.5:c.1871+4345A=	ENSP00000470251.1:n.1871+4345A=
XM_005258821.2:c.1871+4345A=	XP_005258878.1:n.1871+4345A=
XM_005258821.3:c.1871+4345A=	XP_005258878.1:n.1871+4345A=
XM_011526862.1:c.1874+4345A=	XP_011525164.1:n.1874+4345A=
XM_011526862.2:c.1874+4345A=	XP_011525164.1:n.1874+4345A=
XM_011526863.1:c.1871+4345A=	XP_011525165.1:n.1871+4345A=
XM_011526863.2:c.1871+4345A=	XP_011525165.1:n.1871+4345A=
XM_011526864.1:c.1757+4345A=	XP_011525166.1:n.1757+4345A=
XM_011526865.1:c.1874+4345A=	XP_011525167.1:n.1874+4345A=
XM_011526866.1:c.1670+4345A=	XP_011525168.1:n.1670+4345A=
XM_011526867.1:c.1667+4345A=	XP_011525169.1:n.1667+4345A=
XM_011526868.1:c.1631+4345A=	XP_011525170.1:n.1631+4345A=
XM_017026713.1:c.1670+4345A=	XP_016882202.1:n.1670+4345A=
XR_935810.1:n.2418-10146A=
XR_935810.2:n.2422-10146A=