Canonical Allele Identifier: CA1988473488

Gene: EED

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.86261897T= , CM000673.2:g.86261897T=	GRCh38
NC_000011.9:g.85972939T= , CM000673.1:g.85972939T=	GRCh37
NC_000011.8:g.85650587T=	NCBI36
NG_029595.1:g.22134T=

Transcript Alleles

HGVS	Amino-acid Change
NM_003797.5:c.635-2275T= MANE Select	NP_003788.2:n.635-2275T=
ENST00000263360.11:c.635-2275T= MANE Select	ENSP00000263360.6:n.635-2275T=
NM_001308007.1:c.635-2275T=	NP_001294936.1:n.635-2275T=
NM_001308007.2:c.635-2275T=	NP_001294936.1:n.635-2275T=
NM_001330334.1:c.635-2275T=	NP_001317263.1:n.635-2275T=
NM_001330334.2:c.635-2275T=	NP_001317263.1:n.635-2275T=
NM_003797.3:c.635-2275T=	NP_003788.2:n.635-2275T=
NM_003797.4:c.635-2275T=	NP_003788.2:n.635-2275T=
NM_152991.2:c.635-2275T=	NP_694536.1:n.635-2275T=
ENST00000263360.10:c.635-2275T=	ENSP00000263360.6:n.635-2275T=
ENST00000327320.8:c.635-2275T=	ENSP00000315587.4:n.635-2275T=
ENST00000351625.10:c.635-2275T=	ENSP00000338186.5:n.635-2275T=
ENST00000525244.5:n.597-2275T=
ENST00000528180.5:c.635-2275T=	ENSP00000431778.1:n.635-2275T=
ENST00000534595.1:c.111-15083T=
ENST00000672825.1:c.635-2275T=	ENSP00000500834.1:n.635-2275T=
ENST00000673233.2:c.815-2275T=	ENSP00000500914.2:n.815-2275T=
ENST00000707108.1:c.530-2275T=	ENSP00000516737.1:n.530-2275T=
XM_005274373.1:c.635-2275T=	XP_005274430.1:n.635-2275T=
XM_011545330.1:c.635-2275T=	XP_011543632.1:n.635-2275T=
XM_011545330.2:c.635-2275T=	XP_011543632.1:n.635-2275T=
XM_011545331.1:c.635-2275T=	XP_011543633.1:n.635-2275T=
XM_011545331.2:c.635-2275T=	XP_011543633.1:n.635-2275T=
XM_017018512.2:c.635-2275T=	XP_016874001.1:n.635-2275T=
XM_017018513.2:c.635-2275T=	XP_016874002.1:n.635-2275T=
XR_001748022.2:n.1112-2275T=
XR_247215.2:n.1321-2275T=
XR_247215.4:n.1112-2275T=