Canonical Allele Identifier: CA382374107

Gene: MRE11

Linked Data

• MyVariant Identifiers: chr11:g.94169040A>G (hg19) ; chr11:g.94435874A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.94435874A>G , CM000673.2:g.94435874A>G	GRCh38
NC_000011.9:g.94169040A>G , CM000673.1:g.94169040A>G	GRCh37
NC_000011.8:g.93808688A>G	NCBI36
NG_007261.1:g.63001T>C , LRG_85:g.63001T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000323929.8:c.1952T>C MANE Select	ENSP00000325863.4:p.Val651Ala
ENST00000323929.7:c.1952T>C	ENSP00000325863.3:p.Val651Ala
ENST00000323977.7:c.1868T>C	ENSP00000326094.3:p.Val623Ala
ENST00000393241.8:c.1949T>C	ENSP00000376933.4:p.Val650Ala
ENST00000407439.7:c.1961T>C	ENSP00000385614.3:p.Val654Ala
NM_005590.3:c.1868T>C	NP_005581.2:p.Val623Ala
NM_005591.3:c.1952T>C , LRG_85t1:c.1952T>C	NP_005582.1:p.Val651Ala
XM_005274008.2:c.1484T>C	XP_005274065.1:p.Val495Ala
XM_006718842.2:c.1949T>C	XP_006718905.1:p.Val650Ala
XM_011542837.1:c.1952T>C	XP_011541139.1:p.Val651Ala
XR_947828.1:n.2248T>C
NM_001330347.1:c.1949T>C	NP_001317276.1:p.Val650Ala
XM_005274008.3:c.1484T>C	XP_005274065.1:p.Val495Ala
XM_006718842.3:c.1949T>C	XP_006718905.1:p.Val650Ala
XM_011542837.2:c.1952T>C	XP_011541139.1:p.Val651Ala
XM_017017772.1:c.1952T>C	XP_016873261.1:p.Val651Ala
XR_947828.2:n.2248T>C
NM_001330347.2:c.1949T>C	NP_001317276.1:p.Val650Ala
NM_005590.4:c.1868T>C	NP_005581.2:p.Val623Ala
NM_005591.4:c.1952T>C MANE Select	NP_005582.1:p.Val651Ala