Canonical Allele Identifier: CA2615589580
Gene: MRE11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.94476222G>A , CM000673.2:g.94476222G>A GRCh38
NC_000011.9:g.94209388G>A , CM000673.1:g.94209388G>A GRCh37
NC_000011.8:g.93849036G>A NCBI36
NG_007261.1:g.22653C>T , LRG_85:g.22653C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000323929.8:c.659+67C>T MANE Select ENSP00000325863.4:n.659+67C>T
ENST00000323929.7:c.659+67C>T ENSP00000325863.3:n.659+67C>T
ENST00000323977.7:c.659+67C>T ENSP00000326094.3:n.659+67C>T
ENST00000393241.8:c.659+67C>T ENSP00000376933.4:n.659+67C>T
ENST00000407439.7:c.668+67C>T ENSP00000385614.3:n.668+67C>T
ENST00000540013.5:c.659+67C>T ENSP00000440986.1:n.659+67C>T
NM_005590.3:c.659+67C>T NP_005581.2:n.659+67C>T
NM_005591.3:c.659+67C>T , LRG_85t1:c.659+67C>T NP_005582.1:n.659+67C>T
XM_005274008.2:c.191+67C>T XP_005274065.1:n.191+67C>T
XM_006718842.2:c.659+67C>T XP_006718905.1:n.659+67C>T
XM_011542837.1:c.659+67C>T XP_011541139.1:n.659+67C>T
XR_947828.1:n.955+67C>T
NM_001330347.1:c.659+67C>T NP_001317276.1:n.659+67C>T
XM_005274008.3:c.191+67C>T XP_005274065.1:n.191+67C>T
XM_006718842.3:c.659+67C>T XP_006718905.1:n.659+67C>T
XM_011542837.2:c.659+67C>T XP_011541139.1:n.659+67C>T
XM_017017772.1:c.659+67C>T XP_016873261.1:n.659+67C>T
XR_947828.2:n.955+67C>T
NM_001330347.2:c.659+67C>T NP_001317276.1:n.659+67C>T
NM_005590.4:c.659+67C>T NP_005581.2:n.659+67C>T
NM_005591.4:c.659+67C>T MANE Select NP_005582.1:n.659+67C>T