Canonical Allele Identifier: CA682069695

Gene: MRE11

Linked Data

• dbSNP Id: rs1180627741
• gnomAD v3: 11-94476236-AG-A
• gnomAD v4: 11-94476236-AG-A
• MyVariant Identifiers: chr11:g.94209403del (hg19) ; chr11:g.94476237del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.94476237del , CM000673.2:g.94476237del	GRCh38
NC_000011.9:g.94209403del , CM000673.1:g.94209403del	GRCh37
NC_000011.8:g.93849051del	NCBI36
NG_007261.1:g.22638del , LRG_85:g.22638del

Transcript Alleles

HGVS	Amino-acid change
ENST00000323929.8:c.659+52del MANE Select	ENSP00000325863.4:n.659+52del
ENST00000323929.7:c.659+52del	ENSP00000325863.3:n.659+52del
ENST00000323977.7:c.659+52del	ENSP00000326094.3:n.659+52del
ENST00000393241.8:c.659+52del	ENSP00000376933.4:n.659+52del
ENST00000407439.7:c.668+52del	ENSP00000385614.3:n.668+52del
ENST00000540013.5:c.659+52del	ENSP00000440986.1:n.659+52del
NM_005590.3:c.659+52del	NP_005581.2:n.659+52del
NM_005591.3:c.659+52del , LRG_85t1:c.659+52del	NP_005582.1:n.659+52del
XM_005274008.2:c.191+52del	XP_005274065.1:n.191+52del
XM_006718842.2:c.659+52del	XP_006718905.1:n.659+52del
XM_011542837.1:c.659+52del	XP_011541139.1:n.659+52del
XR_947828.1:n.955+52del
NM_001330347.1:c.659+52del	NP_001317276.1:n.659+52del
XM_005274008.3:c.191+52del	XP_005274065.1:n.191+52del
XM_006718842.3:c.659+52del	XP_006718905.1:n.659+52del
XM_011542837.2:c.659+52del	XP_011541139.1:n.659+52del
XM_017017772.1:c.659+52del	XP_016873261.1:n.659+52del
XR_947828.2:n.955+52del
NM_001330347.2:c.659+52del	NP_001317276.1:n.659+52del
NM_005590.4:c.659+52del	NP_005581.2:n.659+52del
NM_005591.4:c.659+52del MANE Select	NP_005582.1:n.659+52del