Canonical Allele Identifier: CA1583252857

Gene: RAD50 TH2LCRR

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132638224G= , CM000667.2:g.132638224G=	GRCh38
NC_000005.9:g.131973916G= , CM000667.1:g.131973916G=	GRCh37
NC_000005.8:g.132001815G=	NCBI36
NG_021151.1:g.86301G=
NG_021151.2:g.86248G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.3618+1G= (RAD50) MANE Select	ENSP00000368100.4:n.3618+1G=
ENST00000638452.2:c.3321+1G=	ENSP00000492349.2:n.3321+1G=
ENST00000638504.1:n.3226+1G=
ENST00000638568.2:c.3321+1G=	ENSP00000491158.2:n.3321+1G=
ENST00000639899.1:n.4137+1G=
ENST00000640655.2:c.3321+1G=	ENSP00000491596.2:n.3321+1G=
ENST00000651249.1:c.454+1G= (RAD50)
ENST00000378823.7:c.3618+1G= (RAD50)	ENSP00000368100.4:n.3618+1G=
ENST00000455677.1:c.253+1G= (RAD50)
ENST00000533482.5:c.*3244+1G= (RAD50)	ENSP00000431225.1:n.*3244+1G=
NM_005732.3:c.3618+1G= (RAD50)	NP_005723.2:n.3618+1G=
NR_132124.1:n.87C= (TH2LCRR)
NR_132125.1:n.231C= (TH2LCRR)
NR_132126.1:n.216C= (TH2LCRR)
XR_427771.1:n.468C= (TH2LCRR)
NM_005732.4:c.3618+1G= (RAD50) MANE Select	NP_005723.2:n.3618+1G=