Canonical Allele Identifier: CA1992461126

Gene: MRE11

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.94459403_94459404delinsCT , CM000673.2:g.94459403_94459404delinsCT	GRCh38
NC_000011.9:g.94192569_94192570delinsCT , CM000673.1:g.94192569_94192570delinsCT	GRCh37
NC_000011.8:g.93832217_93832218delinsCT	NCBI36
NG_007261.1:g.39471_39472delinsAG , LRG_85:g.39471_39472delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323929.8:c.1500+4_1500+5delinsAG MANE Select	ENSP00000325863.4:n.1500+4_1500+5delinsAG
ENST00000323929.7:c.1500+4_1500+5delinsAG	ENSP00000325863.3:n.1500+4_1500+5delinsAG
ENST00000323977.7:c.1500+4_1500+5delinsAG	ENSP00000326094.3:n.1500+4_1500+5delinsAG
ENST00000393241.8:c.1500+4_1500+5delinsAG	ENSP00000376933.4:n.1500+4_1500+5delinsAG
ENST00000407439.7:c.1509+4_1509+5delinsAG	ENSP00000385614.3:n.1509+4_1509+5delinsAG
NM_005590.3:c.1500+4_1500+5delinsAG	NP_005581.2:n.1500+4_1500+5delinsAG
NM_005591.3:c.1500+4_1500+5delinsAG , LRG_85t1:c.1500+4_1500+5delinsAG	NP_005582.1:n.1500+4_1500+5delinsAG
XM_005274008.2:c.1032+4_1032+5delinsAG	XP_005274065.1:n.1032+4_1032+5delinsAG
XM_006718842.2:c.1500+4_1500+5delinsAG	XP_006718905.1:n.1500+4_1500+5delinsAG
XM_011542837.1:c.1500+4_1500+5delinsAG	XP_011541139.1:n.1500+4_1500+5delinsAG
XR_947828.1:n.1796+4_1796+5delinsAG
NM_001330347.1:c.1500+4_1500+5delinsAG	NP_001317276.1:n.1500+4_1500+5delinsAG
XM_005274008.3:c.1032+4_1032+5delinsAG	XP_005274065.1:n.1032+4_1032+5delinsAG
XM_006718842.3:c.1500+4_1500+5delinsAG	XP_006718905.1:n.1500+4_1500+5delinsAG
XM_011542837.2:c.1500+4_1500+5delinsAG	XP_011541139.1:n.1500+4_1500+5delinsAG
XM_017017772.1:c.1500+4_1500+5delinsAG	XP_016873261.1:n.1500+4_1500+5delinsAG
XR_947828.2:n.1796+4_1796+5delinsAG
NM_001330347.2:c.1500+4_1500+5delinsAG	NP_001317276.1:n.1500+4_1500+5delinsAG
NM_005590.4:c.1500+4_1500+5delinsAG	NP_005581.2:n.1500+4_1500+5delinsAG
NM_005591.4:c.1500+4_1500+5delinsAG MANE Select	NP_005582.1:n.1500+4_1500+5delinsAG