Canonical Allele Identifier: CA382372949

Gene: MRE11

Linked Data

• MyVariant Identifiers: chr11:g.94197360T>C (hg19) ; chr11:g.94464194T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.94464194T>C , CM000673.2:g.94464194T>C	GRCh38
NC_000011.9:g.94197360T>C , CM000673.1:g.94197360T>C	GRCh37
NC_000011.8:g.93837008T>C	NCBI36
NG_007261.1:g.34681A>G , LRG_85:g.34681A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323929.8:c.1144A>G MANE Select	ENSP00000325863.4:p.Ser382Gly
ENST00000323929.7:c.1144A>G	ENSP00000325863.3:p.Ser382Gly
ENST00000323977.7:c.1144A>G	ENSP00000326094.3:p.Ser382Gly
ENST00000393241.8:c.1144A>G	ENSP00000376933.4:p.Ser382Gly
ENST00000407439.7:c.1153A>G	ENSP00000385614.3:p.Ser385Gly
NM_005590.3:c.1144A>G	NP_005581.2:p.Ser382Gly
NM_005591.3:c.1144A>G , LRG_85t1:c.1144A>G	NP_005582.1:p.Ser382Gly
XM_005274008.2:c.676A>G	XP_005274065.1:p.Ser226Gly
XM_006718842.2:c.1144A>G	XP_006718905.1:p.Ser382Gly
XM_011542837.1:c.1144A>G	XP_011541139.1:p.Ser382Gly
XR_947828.1:n.1440A>G
NM_001330347.1:c.1144A>G	NP_001317276.1:p.Ser382Gly
XM_005274008.3:c.676A>G	XP_005274065.1:p.Ser226Gly
XM_006718842.3:c.1144A>G	XP_006718905.1:p.Ser382Gly
XM_011542837.2:c.1144A>G	XP_011541139.1:p.Ser382Gly
XM_017017772.1:c.1144A>G	XP_016873261.1:p.Ser382Gly
XR_947828.2:n.1440A>G
NM_001330347.2:c.1144A>G	NP_001317276.1:p.Ser382Gly
NM_005590.4:c.1144A>G	NP_005581.2:p.Ser382Gly
NM_005591.4:c.1144A>G MANE Select	NP_005582.1:p.Ser382Gly