Canonical Allele Identifier: CA2615598591

Gene: MRE11

Linked Data

• gnomAD v4: 11-94435931-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.94435932del , CM000673.2:g.94435932del	GRCh38
NC_000011.9:g.94169098del , CM000673.1:g.94169098del	GRCh37
NC_000011.8:g.93808746del	NCBI36
NG_007261.1:g.62943del , LRG_85:g.62943del

Transcript Alleles

HGVS	Amino-acid change
ENST00000323929.8:c.1927-33del MANE Select	ENSP00000325863.4:n.1927-33del
ENST00000323929.7:c.1927-33del	ENSP00000325863.3:n.1927-33del
ENST00000323977.7:c.1843-33del	ENSP00000326094.3:n.1843-33del
ENST00000393241.8:c.1924-33del	ENSP00000376933.4:n.1924-33del
ENST00000407439.7:c.1936-33del	ENSP00000385614.3:n.1936-33del
NM_005590.3:c.1843-33del	NP_005581.2:n.1843-33del
NM_005591.3:c.1927-33del , LRG_85t1:c.1927-33del	NP_005582.1:n.1927-33del
XM_005274008.2:c.1459-33del	XP_005274065.1:n.1459-33del
XM_006718842.2:c.1924-33del	XP_006718905.1:n.1924-33del
XM_011542837.1:c.1927-33del	XP_011541139.1:n.1927-33del
XR_947828.1:n.2223-33del
NM_001330347.1:c.1924-33del	NP_001317276.1:n.1924-33del
XM_005274008.3:c.1459-33del	XP_005274065.1:n.1459-33del
XM_006718842.3:c.1924-33del	XP_006718905.1:n.1924-33del
XM_011542837.2:c.1927-33del	XP_011541139.1:n.1927-33del
XM_017017772.1:c.1927-33del	XP_016873261.1:n.1927-33del
XR_947828.2:n.2223-33del
NM_001330347.2:c.1924-33del	NP_001317276.1:n.1924-33del
NM_005590.4:c.1843-33del	NP_005581.2:n.1843-33del
NM_005591.4:c.1927-33del MANE Select	NP_005582.1:n.1927-33del