Canonical Allele Identifier: CA941028634

Gene: MRE11

Linked Data

• dbSNP Id: rs1946352469
• gnomAD v3: 11-94459399-GTTAC-G
• gnomAD v4: 11-94459399-GTTAC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.94459404_94459407del , CM000673.2:g.94459404_94459407del	GRCh38
NC_000011.9:g.94192570_94192573del , CM000673.1:g.94192570_94192573del	GRCh37
NC_000011.8:g.93832218_93832221del	NCBI36
NG_007261.1:g.39472_39475del , LRG_85:g.39472_39475del

Transcript Alleles

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