Canonical Allele Identifier: CA2615589229

Gene: MRE11

Linked Data

• gnomAD v4: 11-94464016-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.94464016T>C , CM000673.2:g.94464016T>C	GRCh38
NC_000011.9:g.94197182T>C , CM000673.1:g.94197182T>C	GRCh37
NC_000011.8:g.93836830T>C	NCBI36
NG_007261.1:g.34859A>G , LRG_85:g.34859A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000323929.8:c.1225+97A>G MANE Select	ENSP00000325863.4:n.1225+97A>G
ENST00000323929.7:c.1225+97A>G	ENSP00000325863.3:n.1225+97A>G
ENST00000323977.7:c.1225+97A>G	ENSP00000326094.3:n.1225+97A>G
ENST00000393241.8:c.1225+97A>G	ENSP00000376933.4:n.1225+97A>G
ENST00000407439.7:c.1234+97A>G	ENSP00000385614.3:n.1234+97A>G
NM_005590.3:c.1225+97A>G	NP_005581.2:n.1225+97A>G
NM_005591.3:c.1225+97A>G , LRG_85t1:c.1225+97A>G	NP_005582.1:n.1225+97A>G
XM_005274008.2:c.757+97A>G	XP_005274065.1:n.757+97A>G
XM_006718842.2:c.1225+97A>G	XP_006718905.1:n.1225+97A>G
XM_011542837.1:c.1225+97A>G	XP_011541139.1:n.1225+97A>G
XR_947828.1:n.1521+97A>G
NM_001330347.1:c.1225+97A>G	NP_001317276.1:n.1225+97A>G
XM_005274008.3:c.757+97A>G	XP_005274065.1:n.757+97A>G
XM_006718842.3:c.1225+97A>G	XP_006718905.1:n.1225+97A>G
XM_011542837.2:c.1225+97A>G	XP_011541139.1:n.1225+97A>G
XM_017017772.1:c.1225+97A>G	XP_016873261.1:n.1225+97A>G
XR_947828.2:n.1521+97A>G
NM_001330347.2:c.1225+97A>G	NP_001317276.1:n.1225+97A>G
NM_005590.4:c.1225+97A>G	NP_005581.2:n.1225+97A>G
NM_005591.4:c.1225+97A>G MANE Select	NP_005582.1:n.1225+97A>G