Canonical Allele Identifier: CA1583229755

Gene: RAD50

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132609500G= , CM000667.2:g.132609500G=	GRCh38
NC_000005.9:g.131945192G= , CM000667.1:g.131945192G=	GRCh37
NC_000005.8:g.131973091G=	NCBI36
NG_021151.1:g.57577G=
NG_021151.2:g.57524G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.3036+104G= MANE Select	ENSP00000368100.4:n.3036+104G=
ENST00000638452.2:c.2739+104G=	ENSP00000492349.2:n.2739+104G=
ENST00000638504.1:n.2644+104G=
ENST00000638568.2:c.2739+104G=	ENSP00000491158.2:n.2739+104G=
ENST00000639899.1:n.3555+104G=
ENST00000640655.2:c.2739+104G=	ENSP00000491596.2:n.2739+104G=
ENST00000651723.1:c.*3119+104G=	ENSP00000498237.1:n.*3119+104G=
ENST00000378823.7:c.3036+104G=	ENSP00000368100.4:n.3036+104G=
ENST00000533482.5:c.*2662+104G=	ENSP00000431225.1:n.*2662+104G=
NM_005732.3:c.3036+104G=	NP_005723.2:n.3036+104G=
NM_005732.4:c.3036+104G= MANE Select	NP_005723.2:n.3036+104G=