Canonical Allele Identifier: CA2842557369

Gene: MRE11

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.94476255A>T , CM000673.2:g.94476255A>T	GRCh38
NC_000011.9:g.94209421A>T , CM000673.1:g.94209421A>T	GRCh37
NC_000011.8:g.93849069A>T	NCBI36
NG_007261.1:g.22620T>A , LRG_85:g.22620T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323929.8:c.659+34T>A MANE Select	ENSP00000325863.4:n.659+34T>A
ENST00000323929.7:c.659+34T>A	ENSP00000325863.3:n.659+34T>A
ENST00000323977.7:c.659+34T>A	ENSP00000326094.3:n.659+34T>A
ENST00000393241.8:c.659+34T>A	ENSP00000376933.4:n.659+34T>A
ENST00000407439.7:c.668+34T>A	ENSP00000385614.3:n.668+34T>A
ENST00000540013.5:c.659+34T>A	ENSP00000440986.1:n.659+34T>A
NM_005590.3:c.659+34T>A	NP_005581.2:n.659+34T>A
NM_005591.3:c.659+34T>A , LRG_85t1:c.659+34T>A	NP_005582.1:n.659+34T>A
XM_005274008.2:c.191+34T>A	XP_005274065.1:n.191+34T>A
XM_006718842.2:c.659+34T>A	XP_006718905.1:n.659+34T>A
XM_011542837.1:c.659+34T>A	XP_011541139.1:n.659+34T>A
XR_947828.1:n.955+34T>A
NM_001330347.1:c.659+34T>A	NP_001317276.1:n.659+34T>A
XM_005274008.3:c.191+34T>A	XP_005274065.1:n.191+34T>A
XM_006718842.3:c.659+34T>A	XP_006718905.1:n.659+34T>A
XM_011542837.2:c.659+34T>A	XP_011541139.1:n.659+34T>A
XM_017017772.1:c.659+34T>A	XP_016873261.1:n.659+34T>A
XR_947828.2:n.955+34T>A
NM_001330347.2:c.659+34T>A	NP_001317276.1:n.659+34T>A
NM_005590.4:c.659+34T>A	NP_005581.2:n.659+34T>A
NM_005591.4:c.659+34T>A MANE Select	NP_005582.1:n.659+34T>A