Canonical Allele Identifier: CA226538291

Gene: MRE11

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.94419152T>C , CM000673.2:g.94419152T>C	GRCh38
NC_000011.9:g.94152318T>C , CM000673.1:g.94152318T>C	GRCh37
NC_000011.8:g.93791966T>C	NCBI36
NG_007261.1:g.79723A>G , LRG_85:g.79723A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_005591.4:c.*973A>G MANE Select	NP_005582.1:n.*973A>G
ENST00000323929.8:c.*973A>G MANE Select	ENSP00000325863.4:n.*973A>G
NM_001330347.1:c.*973A>G	NP_001317276.1:n.*973A>G
NM_001330347.2:c.*973A>G	NP_001317276.1:n.*973A>G
NM_005590.3:c.*973A>G	NP_005581.2:n.*973A>G
NM_005590.4:c.*973A>G	NP_005581.2:n.*973A>G
NM_005591.3:c.*973A>G , LRG_85t1:c.*973A>G	NP_005582.1:n.*973A>G
ENST00000323929.7:c.*973A>G	ENSP00000325863.3:n.*973A>G
XM_005274008.3:c.*973A>G	XP_005274065.1:n.*973A>G
XM_006718842.3:c.*973A>G	XP_006718905.1:n.*973A>G
XM_011542837.2:c.*973A>G	XP_011541139.1:n.*973A>G
XM_017017772.1:c.*973A>G	XP_016873261.1:n.*973A>G
XR_947828.1:n.3396A>G
XR_947828.2:n.3396A>G