Canonical Allele Identifier: CA476286742

Gene: MRE11

Linked Data

• MyVariant Identifiers: chr11:g.94209487A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.94476321A>C , CM000673.2:g.94476321A>C	GRCh38
NC_000011.9:g.94209487A>C , CM000673.1:g.94209487A>C	GRCh37
NC_000011.8:g.93849135A>C	NCBI36
NG_007261.1:g.22554T>G , LRG_85:g.22554T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000323929.8:c.627T>G MANE Select	ENSP00000325863.4:p.Ser209=
ENST00000323929.7:c.627T>G	ENSP00000325863.3:p.Ser209=
ENST00000323977.7:c.627T>G	ENSP00000326094.3:p.Ser209=
ENST00000393241.8:c.627T>G	ENSP00000376933.4:p.Ser209=
ENST00000407439.7:c.636T>G	ENSP00000385614.3:p.Ser212=
ENST00000540013.5:c.627T>G	ENSP00000440986.1:p.Ser209=
NM_005590.3:c.627T>G	NP_005581.2:p.Ser209=
NM_005591.3:c.627T>G , LRG_85t1:c.627T>G	NP_005582.1:p.Ser209=
XM_005274008.2:c.159T>G	XP_005274065.1:p.Ser53=
XM_006718842.2:c.627T>G	XP_006718905.1:p.Ser209=
XM_011542837.1:c.627T>G	XP_011541139.1:p.Ser209=
XR_947828.1:n.923T>G
NM_001330347.1:c.627T>G	NP_001317276.1:p.Ser209=
XM_005274008.3:c.159T>G	XP_005274065.1:p.Ser53=
XM_006718842.3:c.627T>G	XP_006718905.1:p.Ser209=
XM_011542837.2:c.627T>G	XP_011541139.1:p.Ser209=
XM_017017772.1:c.627T>G	XP_016873261.1:p.Ser209=
XR_947828.2:n.923T>G
NM_001330347.2:c.627T>G	NP_001317276.1:p.Ser209=
NM_005590.4:c.627T>G	NP_005581.2:p.Ser209=
NM_005591.4:c.627T>G MANE Select	NP_005582.1:p.Ser209=