Canonical Allele Identifier: CA382372843

Gene: MRE11

Linked Data

• MyVariant Identifiers: chr11:g.94197335G>T (hg19) ; chr11:g.94464169G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.94464169G>T , CM000673.2:g.94464169G>T	GRCh38
NC_000011.9:g.94197335G>T , CM000673.1:g.94197335G>T	GRCh37
NC_000011.8:g.93836983G>T	NCBI36
NG_007261.1:g.34706C>A , LRG_85:g.34706C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323929.8:c.1169C>A MANE Select	ENSP00000325863.4:p.Ala390Asp
ENST00000323929.7:c.1169C>A	ENSP00000325863.3:p.Ala390Asp
ENST00000323977.7:c.1169C>A	ENSP00000326094.3:p.Ala390Asp
ENST00000393241.8:c.1169C>A	ENSP00000376933.4:p.Ala390Asp
ENST00000407439.7:c.1178C>A	ENSP00000385614.3:p.Ala393Asp
NM_005590.3:c.1169C>A	NP_005581.2:p.Ala390Asp
NM_005591.3:c.1169C>A , LRG_85t1:c.1169C>A	NP_005582.1:p.Ala390Asp
XM_005274008.2:c.701C>A	XP_005274065.1:p.Ala234Asp
XM_006718842.2:c.1169C>A	XP_006718905.1:p.Ala390Asp
XM_011542837.1:c.1169C>A	XP_011541139.1:p.Ala390Asp
XR_947828.1:n.1465C>A
NM_001330347.1:c.1169C>A	NP_001317276.1:p.Ala390Asp
XM_005274008.3:c.701C>A	XP_005274065.1:p.Ala234Asp
XM_006718842.3:c.1169C>A	XP_006718905.1:p.Ala390Asp
XM_011542837.2:c.1169C>A	XP_011541139.1:p.Ala390Asp
XM_017017772.1:c.1169C>A	XP_016873261.1:p.Ala390Asp
XR_947828.2:n.1465C>A
NM_001330347.2:c.1169C>A	NP_001317276.1:p.Ala390Asp
NM_005590.4:c.1169C>A	NP_005581.2:p.Ala390Asp
NM_005591.4:c.1169C>A MANE Select	NP_005582.1:p.Ala390Asp