Canonical Allele Identifier: CA476287105

Gene: MRE11

Linked Data

• MyVariant Identifiers: chr11:g.94169012T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.94435846T>A , CM000673.2:g.94435846T>A	GRCh38
NC_000011.9:g.94169012T>A , CM000673.1:g.94169012T>A	GRCh37
NC_000011.8:g.93808660T>A	NCBI36
NG_007261.1:g.63029A>T , LRG_85:g.63029A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000323929.8:c.1980A>T MANE Select	ENSP00000325863.4:p.Ser660=
ENST00000323929.7:c.1980A>T	ENSP00000325863.3:p.Ser660=
ENST00000323977.7:c.1896A>T	ENSP00000326094.3:p.Ser632=
ENST00000393241.8:c.1977A>T	ENSP00000376933.4:p.Ser659=
ENST00000407439.7:c.1989A>T	ENSP00000385614.3:p.Ser663=
NM_005590.3:c.1896A>T	NP_005581.2:p.Ser632=
NM_005591.3:c.1980A>T , LRG_85t1:c.1980A>T	NP_005582.1:p.Ser660=
XM_005274008.2:c.1512A>T	XP_005274065.1:p.Ser504=
XM_006718842.2:c.1977A>T	XP_006718905.1:p.Ser659=
XM_011542837.1:c.1980A>T	XP_011541139.1:p.Ser660=
XR_947828.1:n.2276A>T
NM_001330347.1:c.1977A>T	NP_001317276.1:p.Ser659=
XM_005274008.3:c.1512A>T	XP_005274065.1:p.Ser504=
XM_006718842.3:c.1977A>T	XP_006718905.1:p.Ser659=
XM_011542837.2:c.1980A>T	XP_011541139.1:p.Ser660=
XM_017017772.1:c.1980A>T	XP_016873261.1:p.Ser660=
XR_947828.2:n.2276A>T
NM_001330347.2:c.1977A>T	NP_001317276.1:p.Ser659=
NM_005590.4:c.1896A>T	NP_005581.2:p.Ser632=
NM_005591.4:c.1980A>T MANE Select	NP_005582.1:p.Ser660=