Canonical Allele Identifier: CA446364107

Gene: RAD50

Linked Data

• MyVariant Identifiers: chr5:g.131940583A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132604891A>G , CM000667.2:g.132604891A>G	GRCh38
NC_000005.9:g.131940583A>G , CM000667.1:g.131940583A>G	GRCh37
NC_000005.8:g.131968482A>G	NCBI36
NG_021151.1:g.52968A>G
NG_021151.2:g.52915A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.2610A>G MANE Select	ENSP00000368100.4:p.Leu870=
ENST00000638452.2:c.2313A>G	ENSP00000492349.2:p.Leu771=
ENST00000638504.1:n.2218A>G
ENST00000638568.2:c.2313A>G	ENSP00000491158.2:p.Leu771=
ENST00000639899.1:n.3129A>G
ENST00000640655.2:c.2313A>G	ENSP00000491596.2:p.Leu771=
ENST00000651160.1:c.*754A>G	ENSP00000498829.1:n.*754A>G
ENST00000651723.1:c.*2693A>G	ENSP00000498237.1:n.*2693A>G
ENST00000652016.1:c.*827A>G	ENSP00000498267.1:n.*827A>G
ENST00000652485.1:c.2643A>G	ENSP00000498973.1:p.Leu881=
ENST00000378823.7:c.2610A>G	ENSP00000368100.4:p.Leu870=
ENST00000423956.5:c.*796A>G	ENSP00000390971.1:n.*796A>G
ENST00000533482.5:c.*2236A>G	ENSP00000431225.1:n.*2236A>G
NM_005732.3:c.2610A>G	NP_005723.2:p.Leu870=
NM_005732.4:c.2610A>G MANE Select	NP_005723.2:p.Leu870=