Canonical Allele Identifier: CA16613506

Gene: MRE11

Linked Data

• ClinVar Variation Id: 414692
• ClinVar RCV Id: RCV000473385 ; RCV003899968
• dbSNP Id: rs1060504336
• gnomAD v2: 11-94169074-G-T
• gnomAD v3: 11-94435908-G-T
• gnomAD v4: 11-94435908-G-T
• MyVariant Identifiers: chr11:g.94169074G>T (hg19) ; chr11:g.94435908G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.94435908G>T , CM000673.2:g.94435908G>T	GRCh38
NC_000011.9:g.94169074G>T , CM000673.1:g.94169074G>T	GRCh37
NC_000011.8:g.93808722G>T	NCBI36
NG_007261.1:g.62967C>A , LRG_85:g.62967C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000323929.8:c.1927-9C>A MANE Select	ENSP00000325863.4:n.1927-9C>A
ENST00000323929.7:c.1927-9C>A	ENSP00000325863.3:n.1927-9C>A
ENST00000323977.7:c.1843-9C>A	ENSP00000326094.3:n.1843-9C>A
ENST00000393241.8:c.1924-9C>A	ENSP00000376933.4:n.1924-9C>A
ENST00000407439.7:c.1936-9C>A	ENSP00000385614.3:n.1936-9C>A
NM_005590.3:c.1843-9C>A	NP_005581.2:n.1843-9C>A
NM_005591.3:c.1927-9C>A , LRG_85t1:c.1927-9C>A	NP_005582.1:n.1927-9C>A
XM_005274008.2:c.1459-9C>A	XP_005274065.1:n.1459-9C>A
XM_006718842.2:c.1924-9C>A	XP_006718905.1:n.1924-9C>A
XM_011542837.1:c.1927-9C>A	XP_011541139.1:n.1927-9C>A
XR_947828.1:n.2223-9C>A
NM_001330347.1:c.1924-9C>A	NP_001317276.1:n.1924-9C>A
XM_005274008.3:c.1459-9C>A	XP_005274065.1:n.1459-9C>A
XM_006718842.3:c.1924-9C>A	XP_006718905.1:n.1924-9C>A
XM_011542837.2:c.1927-9C>A	XP_011541139.1:n.1927-9C>A
XM_017017772.1:c.1927-9C>A	XP_016873261.1:n.1927-9C>A
XR_947828.2:n.2223-9C>A
NM_001330347.2:c.1924-9C>A	NP_001317276.1:n.1924-9C>A
NM_005590.4:c.1843-9C>A	NP_005581.2:n.1843-9C>A
NM_005591.4:c.1927-9C>A MANE Select	NP_005582.1:n.1927-9C>A