Canonical Allele Identifier: CA382004688

Gene: EED

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.86266123T>C , CM000673.2:g.86266123T>C	GRCh38
NC_000011.9:g.85977165T>C , CM000673.1:g.85977165T>C	GRCh37
NC_000011.8:g.85654813T>C	NCBI36
NG_029595.1:g.26360T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_003797.5:c.767T>C MANE Select	NP_003788.2:p.Met256Thr
ENST00000263360.11:c.767T>C MANE Select	ENSP00000263360.6:p.Met256Thr
NM_001308007.1:c.767T>C	NP_001294936.1:p.Met256Thr
NM_001308007.2:c.767T>C	NP_001294936.1:p.Met256Thr
NM_001330334.1:c.726+1860T>C	NP_001317263.1:n.726+1860T>C
NM_001330334.2:c.726+1860T>C	NP_001317263.1:n.726+1860T>C
NM_003797.3:c.767T>C	NP_003788.2:p.Met256Thr
NM_003797.4:c.767T>C	NP_003788.2:p.Met256Thr
NM_152991.2:c.767T>C	NP_694536.1:p.Met256Thr
ENST00000263360.10:c.767T>C	ENSP00000263360.6:p.Met256Thr
ENST00000327320.8:c.767T>C	ENSP00000315587.4:p.Met256Thr
ENST00000351625.10:c.767T>C	ENSP00000338186.5:p.Met256Thr
ENST00000525244.5:n.729T>C
ENST00000528180.5:c.726+1860T>C	ENSP00000431778.1:n.726+1860T>C
ENST00000533228.1:n.360T>C
ENST00000534564.5:n.2179T>C
ENST00000534595.1:c.111-10857T>C
ENST00000672825.1:c.767T>C	ENSP00000500834.1:p.Met256Thr
ENST00000673233.2:c.947T>C	ENSP00000500914.2:p.Met316Thr
ENST00000707108.1:c.662T>C	ENSP00000516737.1:p.Met221Thr
XM_005274373.1:c.726+1860T>C	XP_005274430.1:n.726+1860T>C
XM_011545330.1:c.767T>C	XP_011543632.1:p.Met256Thr
XM_011545330.2:c.767T>C	XP_011543632.1:p.Met256Thr
XM_011545331.1:c.767T>C	XP_011543633.1:p.Met256Thr
XM_011545331.2:c.767T>C	XP_011543633.1:p.Met256Thr
XM_017018512.2:c.767T>C	XP_016874001.1:p.Met256Thr
XM_017018513.2:c.726+1860T>C	XP_016874002.1:n.726+1860T>C
XR_001748022.2:n.1244T>C
XR_247215.2:n.1453T>C
XR_247215.4:n.1244T>C