Canonical Allele Identifier: CA382366960

Gene: MRE11

Linked Data

• MyVariant Identifiers: chr11:g.94179059G>C (hg19) ; chr11:g.94445893G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.94445893G>C , CM000673.2:g.94445893G>C	GRCh38
NC_000011.9:g.94179059G>C , CM000673.1:g.94179059G>C	GRCh37
NC_000011.8:g.93818707G>C	NCBI36
NG_007261.1:g.52982C>G , LRG_85:g.52982C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000323929.8:c.1784C>G MANE Select	ENSP00000325863.4:p.Ala595Gly
ENST00000323929.7:c.1784C>G	ENSP00000325863.3:p.Ala595Gly
ENST00000323977.7:c.1783+1326C>G	ENSP00000326094.3:n.1783+1326C>G
ENST00000393241.8:c.1784-3C>G	ENSP00000376933.4:n.1784-3C>G
ENST00000407439.7:c.1793C>G	ENSP00000385614.3:p.Ala598Gly
ENST00000535120.1:n.83-3C>G
NM_005590.3:c.1783+1326C>G	NP_005581.2:n.1783+1326C>G
NM_005591.3:c.1784C>G , LRG_85t1:c.1784C>G	NP_005582.1:p.Ala595Gly
XM_005274008.2:c.1316C>G	XP_005274065.1:p.Ala439Gly
XM_006718842.2:c.1784-3C>G	XP_006718905.1:n.1784-3C>G
XM_011542837.1:c.1784C>G	XP_011541139.1:p.Ala595Gly
XR_947828.1:n.2080C>G
NM_001330347.1:c.1784-3C>G	NP_001317276.1:n.1784-3C>G
XM_005274008.3:c.1316C>G	XP_005274065.1:p.Ala439Gly
XM_006718842.3:c.1784-3C>G	XP_006718905.1:n.1784-3C>G
XM_011542837.2:c.1784C>G	XP_011541139.1:p.Ala595Gly
XM_017017772.1:c.1784C>G	XP_016873261.1:p.Ala595Gly
XR_947828.2:n.2080C>G
NM_001330347.2:c.1784-3C>G	NP_001317276.1:n.1784-3C>G
NM_005590.4:c.1783+1326C>G	NP_005581.2:n.1783+1326C>G
NM_005591.4:c.1784C>G MANE Select	NP_005582.1:p.Ala595Gly