Canonical Allele Identifier: CA1992471827

Gene: MRE11

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.94466374A= , CM000673.2:g.94466374A=	GRCh38
NC_000011.9:g.94199540A= , CM000673.1:g.94199540A=	GRCh37
NC_000011.8:g.93839188A=	NCBI36
NG_007261.1:g.32501T= , LRG_85:g.32501T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323929.8:c.1098+1439T= MANE Select	ENSP00000325863.4:n.1098+1439T=
ENST00000323929.7:c.1098+1439T=	ENSP00000325863.3:n.1098+1439T=
ENST00000323977.7:c.1098+1439T=	ENSP00000326094.3:n.1098+1439T=
ENST00000393241.8:c.1098+1439T=	ENSP00000376933.4:n.1098+1439T=
ENST00000407439.7:c.1107+1439T=	ENSP00000385614.3:n.1107+1439T=
NM_005590.3:c.1098+1439T=	NP_005581.2:n.1098+1439T=
NM_005591.3:c.1098+1439T= , LRG_85t1:c.1098+1439T=	NP_005582.1:n.1098+1439T=
XM_005274008.2:c.630+1439T=	XP_005274065.1:n.630+1439T=
XM_006718842.2:c.1098+1439T=	XP_006718905.1:n.1098+1439T=
XM_011542837.1:c.1098+1439T=	XP_011541139.1:n.1098+1439T=
XR_947828.1:n.1394+1439T=
NM_001330347.1:c.1098+1439T=	NP_001317276.1:n.1098+1439T=
XM_005274008.3:c.630+1439T=	XP_005274065.1:n.630+1439T=
XM_006718842.3:c.1098+1439T=	XP_006718905.1:n.1098+1439T=
XM_011542837.2:c.1098+1439T=	XP_011541139.1:n.1098+1439T=
XM_017017772.1:c.1098+1439T=	XP_016873261.1:n.1098+1439T=
XR_947828.2:n.1394+1439T=
NM_001330347.2:c.1098+1439T=	NP_001317276.1:n.1098+1439T=
NM_005590.4:c.1098+1439T=	NP_005581.2:n.1098+1439T=
NM_005591.4:c.1098+1439T= MANE Select	NP_005582.1:n.1098+1439T=