Canonical Allele Identifier: CA476281831

Gene: MRE11

Linked Data

• MyVariant Identifiers: chr11:g.94192533_94192536del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.94459367_94459370del , CM000673.2:g.94459367_94459370del	GRCh38
NC_000011.9:g.94192533_94192536del , CM000673.1:g.94192533_94192536del	GRCh37
NC_000011.8:g.93832181_93832184del	NCBI36
NG_007261.1:g.39505_39508del , LRG_85:g.39505_39508del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323929.8:c.1500+38_1500+41del MANE Select	ENSP00000325863.4:n.1500+38_1500+41del
ENST00000323929.7:c.1500+38_1500+41del	ENSP00000325863.3:n.1500+38_1500+41del
ENST00000323977.7:c.1500+38_1500+41del	ENSP00000326094.3:n.1500+38_1500+41del
ENST00000393241.8:c.1500+38_1500+41del	ENSP00000376933.4:n.1500+38_1500+41del
ENST00000407439.7:c.1509+38_1509+41del	ENSP00000385614.3:n.1509+38_1509+41del
NM_005590.3:c.1500+38_1500+41del	NP_005581.2:n.1500+38_1500+41del
NM_005591.3:c.1500+38_1500+41del , LRG_85t1:c.1500+38_1500+41del	NP_005582.1:n.1500+38_1500+41del
XM_005274008.2:c.1032+38_1032+41del	XP_005274065.1:n.1032+38_1032+41del
XM_006718842.2:c.1500+38_1500+41del	XP_006718905.1:n.1500+38_1500+41del
XM_011542837.1:c.1500+38_1500+41del	XP_011541139.1:n.1500+38_1500+41del
XR_947828.1:n.1796+38_1796+41del
NM_001330347.1:c.1500+38_1500+41del	NP_001317276.1:n.1500+38_1500+41del
XM_005274008.3:c.1032+38_1032+41del	XP_005274065.1:n.1032+38_1032+41del
XM_006718842.3:c.1500+38_1500+41del	XP_006718905.1:n.1500+38_1500+41del
XM_011542837.2:c.1500+38_1500+41del	XP_011541139.1:n.1500+38_1500+41del
XM_017017772.1:c.1500+38_1500+41del	XP_016873261.1:n.1500+38_1500+41del
XR_947828.2:n.1796+38_1796+41del
NM_001330347.2:c.1500+38_1500+41del	NP_001317276.1:n.1500+38_1500+41del
NM_005590.4:c.1500+38_1500+41del	NP_005581.2:n.1500+38_1500+41del
NM_005591.4:c.1500+38_1500+41del MANE Select	NP_005582.1:n.1500+38_1500+41del