Canonical Allele Identifier: CA1583233422

Gene: RAD50

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132618005_132618006delinsCT , CM000667.2:g.132618005_132618006delinsCT	GRCh38
NC_000005.9:g.131953697_131953698delinsCT , CM000667.1:g.131953697_131953698delinsCT	GRCh37
NC_000005.8:g.131981596_131981597delinsCT	NCBI36
NG_021151.1:g.66082_66083delinsCT
NG_021151.2:g.66029_66030delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000378823.8:c.3165-65_3165-64delinsCT MANE Select	ENSP00000368100.4:n.3165-65_3165-64delinsCT
ENST00000638452.2:c.2868-65_2868-64delinsCT	ENSP00000492349.2:n.2868-65_2868-64delinsCT
ENST00000638504.1:n.2773-65_2773-64delinsCT
ENST00000638568.2:c.2868-65_2868-64delinsCT	ENSP00000491158.2:n.2868-65_2868-64delinsCT
ENST00000639899.1:n.3684-65_3684-64delinsCT
ENST00000640655.2:c.2868-65_2868-64delinsCT	ENSP00000491596.2:n.2868-65_2868-64delinsCT
ENST00000378823.7:c.3165-65_3165-64delinsCT	ENSP00000368100.4:n.3165-65_3165-64delinsCT
ENST00000533482.5:c.*2791-65_*2791-64delinsCT	ENSP00000431225.1:n.*2791-65_*2791-64delinsCT
NM_005732.3:c.3165-65_3165-64delinsCT	NP_005723.2:n.3165-65_3165-64delinsCT
NM_005732.4:c.3165-65_3165-64delinsCT MANE Select	NP_005723.2:n.3165-65_3165-64delinsCT