Canonical Allele Identifier: CA127260825

Gene: RAD50

Linked Data

• dbSNP Id: rs1129482
• MyVariant Identifiers: chr5:g.131944897A>T (hg19) ; chr5:g.132609205A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132609205A>T , CM000667.2:g.132609205A>T	GRCh38
NC_000005.9:g.131944897A>T , CM000667.1:g.131944897A>T	GRCh37
NC_000005.8:g.131972796A>T	NCBI36
NG_021151.1:g.57282A>T
NG_021151.2:g.57229A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.2918A>T MANE Select	ENSP00000368100.4:p.Lys973Met
ENST00000638452.2:c.2621A>T	ENSP00000492349.2:p.Lys874Met
ENST00000638504.1:n.2526A>T
ENST00000638568.2:c.2621A>T	ENSP00000491158.2:p.Lys874Met
ENST00000639899.1:n.3437A>T
ENST00000640655.2:c.2621A>T	ENSP00000491596.2:p.Lys874Met
ENST00000651160.1:c.*1062A>T	ENSP00000498829.1:n.*1062A>T
ENST00000651723.1:c.*3001A>T	ENSP00000498237.1:n.*3001A>T
ENST00000378823.7:c.2918A>T	ENSP00000368100.4:p.Lys973Met
ENST00000423956.5:c.*1104A>T	ENSP00000390971.1:n.*1104A>T
ENST00000533482.5:c.*2544A>T	ENSP00000431225.1:n.*2544A>T
NM_005732.3:c.2918A>T	NP_005723.2:p.Lys973Met
NM_005732.4:c.2918A>T MANE Select	NP_005723.2:p.Lys973Met