Canonical Allele Identifier: CA360955307

Gene: RAD50

Linked Data

• MyVariant Identifiers: chr5:g.131939617A>T (hg19) ; chr5:g.132603925A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132603925A>T , CM000667.2:g.132603925A>T	GRCh38
NC_000005.9:g.131939617A>T , CM000667.1:g.131939617A>T	GRCh37
NC_000005.8:g.131967516A>T	NCBI36
NG_021151.1:g.52002A>T
NG_021151.2:g.51949A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000378823.8:c.2403A>T MANE Select	ENSP00000368100.4:p.Glu801Asp
ENST00000638452.2:c.2106A>T	ENSP00000492349.2:p.Glu702Asp
ENST00000638504.1:n.2011A>T
ENST00000638568.2:c.2106A>T	ENSP00000491158.2:p.Glu702Asp
ENST00000639899.1:n.2922A>T
ENST00000640655.2:c.2106A>T	ENSP00000491596.2:p.Glu702Asp
ENST00000651160.1:c.*547A>T	ENSP00000498829.1:n.*547A>T
ENST00000651658.1:n.2946A>T
ENST00000651723.1:c.*2486A>T	ENSP00000498237.1:n.*2486A>T
ENST00000652016.1:c.*620A>T	ENSP00000498267.1:n.*620A>T
ENST00000652485.1:c.2436A>T	ENSP00000498973.1:p.Glu812Asp
ENST00000378823.7:c.2403A>T	ENSP00000368100.4:p.Glu801Asp
ENST00000423956.5:c.*589A>T	ENSP00000390971.1:n.*589A>T
ENST00000533482.5:c.*2029A>T	ENSP00000431225.1:n.*2029A>T
NM_005732.3:c.2403A>T	NP_005723.2:p.Glu801Asp
NM_005732.4:c.2403A>T MANE Select	NP_005723.2:p.Glu801Asp