Canonical Allele Identifier: CA2615598507

Gene: MRE11

Linked Data

• gnomAD v4: 11-94435811-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.94435811G>T , CM000673.2:g.94435811G>T	GRCh38
NC_000011.9:g.94168977G>T , CM000673.1:g.94168977G>T	GRCh37
NC_000011.8:g.93808625G>T	NCBI36
NG_007261.1:g.63064C>A , LRG_85:g.63064C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000323929.8:c.1994+21C>A MANE Select	ENSP00000325863.4:n.1994+21C>A
ENST00000323929.7:c.1994+21C>A	ENSP00000325863.3:n.1994+21C>A
ENST00000323977.7:c.1910+21C>A	ENSP00000326094.3:n.1910+21C>A
ENST00000393241.8:c.1991+21C>A	ENSP00000376933.4:n.1991+21C>A
ENST00000407439.7:c.2003+21C>A	ENSP00000385614.3:n.2003+21C>A
NM_005590.3:c.1910+21C>A	NP_005581.2:n.1910+21C>A
NM_005591.3:c.1994+21C>A , LRG_85t1:c.1994+21C>A	NP_005582.1:n.1994+21C>A
XM_005274008.2:c.1526+21C>A	XP_005274065.1:n.1526+21C>A
XM_006718842.2:c.1991+21C>A	XP_006718905.1:n.1991+21C>A
XM_011542837.1:c.1994+21C>A	XP_011541139.1:n.1994+21C>A
XR_947828.1:n.2290+21C>A
NM_001330347.1:c.1991+21C>A	NP_001317276.1:n.1991+21C>A
XM_005274008.3:c.1526+21C>A	XP_005274065.1:n.1526+21C>A
XM_006718842.3:c.1991+21C>A	XP_006718905.1:n.1991+21C>A
XM_011542837.2:c.1994+21C>A	XP_011541139.1:n.1994+21C>A
XM_017017772.1:c.1994+21C>A	XP_016873261.1:n.1994+21C>A
XR_947828.2:n.2290+21C>A
NM_001330347.2:c.1991+21C>A	NP_001317276.1:n.1991+21C>A
NM_005590.4:c.1910+21C>A	NP_005581.2:n.1910+21C>A
NM_005591.4:c.1994+21C>A MANE Select	NP_005582.1:n.1994+21C>A