Canonical Allele Identifier: CA476282688

Gene: MRE11 MIR548L

Linked Data

• MyVariant Identifiers: chr11:g.94199712A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.94466546A>T , CM000673.2:g.94466546A>T	GRCh38
NC_000011.9:g.94199712A>T , CM000673.1:g.94199712A>T	GRCh37
NC_000011.8:g.93839360A>T	NCBI36
NG_007261.1:g.32329T>A , LRG_85:g.32329T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000323929.8:c.1098+1267T>A (MRE11) MANE Select	ENSP00000325863.4:n.1098+1267T>A
ENST00000323929.7:c.1098+1267T>A (MRE11)	ENSP00000325863.3:n.1098+1267T>A
ENST00000323977.7:c.1098+1267T>A (MRE11)	ENSP00000326094.3:n.1098+1267T>A
ENST00000393241.8:c.1098+1267T>A (MRE11)	ENSP00000376933.4:n.1098+1267T>A
ENST00000407439.7:c.1107+1267T>A (MRE11)	ENSP00000385614.3:n.1107+1267T>A
NM_005590.3:c.1098+1267T>A (MRE11)	NP_005581.2:n.1098+1267T>A
NM_005591.3:c.1098+1267T>A , LRG_85t1:c.1098+1267T>A (MRE11)	NP_005582.1:n.1098+1267T>A
NR_031630.1:n.35T>A (MIR548L)
XM_005274008.2:c.630+1267T>A (MRE11)	XP_005274065.1:n.630+1267T>A
XM_006718842.2:c.1098+1267T>A (MRE11)	XP_006718905.1:n.1098+1267T>A
XM_011542837.1:c.1098+1267T>A (MRE11)	XP_011541139.1:n.1098+1267T>A
XR_947828.1:n.1394+1267T>A (MRE11)
NM_001330347.1:c.1098+1267T>A (MRE11)	NP_001317276.1:n.1098+1267T>A
XM_005274008.3:c.630+1267T>A (MRE11)	XP_005274065.1:n.630+1267T>A
XM_006718842.3:c.1098+1267T>A (MRE11)	XP_006718905.1:n.1098+1267T>A
XM_011542837.2:c.1098+1267T>A (MRE11)	XP_011541139.1:n.1098+1267T>A
XM_017017772.1:c.1098+1267T>A (MRE11)	XP_016873261.1:n.1098+1267T>A
XR_947828.2:n.1394+1267T>A (MRE11)
NM_001330347.2:c.1098+1267T>A (MRE11)	NP_001317276.1:n.1098+1267T>A
NM_005590.4:c.1098+1267T>A (MRE11)	NP_005581.2:n.1098+1267T>A
NM_005591.4:c.1098+1267T>A (MRE11) MANE Select	NP_005582.1:n.1098+1267T>A