Canonical Allele Identifier: CA650290455

Gene: RAD50

Linked Data

• COSMIC: COSN23528016

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132588561dup , CM000667.2:g.132588561dup	GRCh38
NC_000005.9:g.131924253dup , CM000667.1:g.131924253dup	GRCh37
NC_000005.8:g.131952152dup	NCBI36
NG_021151.1:g.36638dup
NG_021151.2:g.36585dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.1052-126dup MANE Select	ENSP00000368100.4:n.1052-126dup
ENST00000638452.2:c.755-126dup	ENSP00000492349.2:n.755-126dup
ENST00000638504.1:n.738-126dup
ENST00000638568.2:c.755-126dup	ENSP00000491158.2:n.755-126dup
ENST00000639899.1:n.1571-126dup
ENST00000640655.2:c.755-126dup	ENSP00000491596.2:n.755-126dup
ENST00000651160.1:c.1052-126dup	ENSP00000498829.1:n.1052-126dup
ENST00000651541.1:c.755-126dup	ENSP00000498795.1:n.755-126dup
ENST00000651658.1:n.1479-126dup
ENST00000651723.1:c.*1135-126dup	ENSP00000498237.1:n.*1135-126dup
ENST00000652016.1:c.1052-126dup	ENSP00000498267.1:n.1052-126dup
ENST00000652485.1:c.1052-126dup	ENSP00000498973.1:n.1052-126dup
ENST00000378823.7:c.1052-126dup	ENSP00000368100.4:n.1052-126dup
ENST00000423956.5:c.1052-126dup	ENSP00000390971.1:n.1052-126dup
ENST00000453394.5:c.1052-126dup	ENSP00000400049.1:n.1052-126dup
ENST00000487596.1:n.618-126dup
ENST00000533482.5:c.*678-126dup	ENSP00000431225.1:n.*678-126dup
NM_005732.3:c.1052-126dup	NP_005723.2:n.1052-126dup
NM_005732.4:c.1052-126dup MANE Select	NP_005723.2:n.1052-126dup