Canonical Allele Identifier: CA382366900

Gene: MRE11

Linked Data

• MyVariant Identifiers: chr11:g.94179053G>T (hg19) ; chr11:g.94445887G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.94445887G>T , CM000673.2:g.94445887G>T	GRCh38
NC_000011.9:g.94179053G>T , CM000673.1:g.94179053G>T	GRCh37
NC_000011.8:g.93818701G>T	NCBI36
NG_007261.1:g.52988C>A , LRG_85:g.52988C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323929.8:c.1790C>A MANE Select	ENSP00000325863.4:p.Thr597Asn
ENST00000323929.7:c.1790C>A	ENSP00000325863.3:p.Thr597Asn
ENST00000323977.7:c.1783+1332C>A	ENSP00000326094.3:n.1783+1332C>A
ENST00000393241.8:c.1787C>A	ENSP00000376933.4:p.Thr596Asn
ENST00000407439.7:c.1799C>A	ENSP00000385614.3:p.Thr600Asn
ENST00000535120.1:n.86C>A
NM_005590.3:c.1783+1332C>A	NP_005581.2:n.1783+1332C>A
NM_005591.3:c.1790C>A , LRG_85t1:c.1790C>A	NP_005582.1:p.Thr597Asn
XM_005274008.2:c.1322C>A	XP_005274065.1:p.Thr441Asn
XM_006718842.2:c.1787C>A	XP_006718905.1:p.Thr596Asn
XM_011542837.1:c.1790C>A	XP_011541139.1:p.Thr597Asn
XR_947828.1:n.2086C>A
NM_001330347.1:c.1787C>A	NP_001317276.1:p.Thr596Asn
XM_005274008.3:c.1322C>A	XP_005274065.1:p.Thr441Asn
XM_006718842.3:c.1787C>A	XP_006718905.1:p.Thr596Asn
XM_011542837.2:c.1790C>A	XP_011541139.1:p.Thr597Asn
XM_017017772.1:c.1790C>A	XP_016873261.1:p.Thr597Asn
XR_947828.2:n.2086C>A
NM_001330347.2:c.1787C>A	NP_001317276.1:p.Thr596Asn
NM_005590.4:c.1783+1332C>A	NP_005581.2:n.1783+1332C>A
NM_005591.4:c.1790C>A MANE Select	NP_005582.1:p.Thr597Asn