Canonical Allele Identifier: CA941023267

Gene: MRE11

Linked Data

• dbSNP Id: rs1945930167
• gnomAD v3: 11-94446323-CTT-C
• gnomAD v4: 11-94446323-CTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.94446324_94446325del , CM000673.2:g.94446324_94446325del	GRCh38
NC_000011.9:g.94179490_94179491del , CM000673.1:g.94179490_94179491del	GRCh37
NC_000011.8:g.93819138_93819139del	NCBI36
NG_007261.1:g.52550_52551del , LRG_85:g.52550_52551del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323929.8:c.1784-432_1784-431del MANE Select	ENSP00000325863.4:n.1784-432_1784-431del
ENST00000323929.7:c.1784-432_1784-431del	ENSP00000325863.3:n.1784-432_1784-431del
ENST00000323977.7:c.1783+894_1783+895del	ENSP00000326094.3:n.1783+894_1783+895del
ENST00000393241.8:c.1784-435_1784-434del	ENSP00000376933.4:n.1784-435_1784-434del
ENST00000407439.7:c.1793-432_1793-431del	ENSP00000385614.3:n.1793-432_1793-431del
ENST00000535120.1:n.83-435_83-434del
NM_005590.3:c.1783+894_1783+895del	NP_005581.2:n.1783+894_1783+895del
NM_005591.3:c.1784-432_1784-431del , LRG_85t1:c.1784-432_1784-431del	NP_005582.1:n.1784-432_1784-431del
XM_005274008.2:c.1316-432_1316-431del	XP_005274065.1:n.1316-432_1316-431del
XM_006718842.2:c.1784-435_1784-434del	XP_006718905.1:n.1784-435_1784-434del
XM_011542837.1:c.1784-432_1784-431del	XP_011541139.1:n.1784-432_1784-431del
XR_947828.1:n.2080-432_2080-431del
NM_001330347.1:c.1784-435_1784-434del	NP_001317276.1:n.1784-435_1784-434del
XM_005274008.3:c.1316-432_1316-431del	XP_005274065.1:n.1316-432_1316-431del
XM_006718842.3:c.1784-435_1784-434del	XP_006718905.1:n.1784-435_1784-434del
XM_011542837.2:c.1784-432_1784-431del	XP_011541139.1:n.1784-432_1784-431del
XM_017017772.1:c.1784-432_1784-431del	XP_016873261.1:n.1784-432_1784-431del
XR_947828.2:n.2080-432_2080-431del
NM_001330347.2:c.1784-435_1784-434del	NP_001317276.1:n.1784-435_1784-434del
NM_005590.4:c.1783+894_1783+895del	NP_005581.2:n.1783+894_1783+895del
NM_005591.4:c.1784-432_1784-431del MANE Select	NP_005582.1:n.1784-432_1784-431del