Canonical Allele Identifier: CA1583240571

Gene: RAD50

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132591875A= , CM000667.2:g.132591875A=	GRCh38
NC_000005.9:g.131927567A= , CM000667.1:g.131927567A=	GRCh37
NC_000005.8:g.131955466A=	NCBI36
NG_021151.1:g.39952A=
NG_021151.2:g.39899A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000378823.8:c.1636-2A= MANE Select	ENSP00000368100.4:n.1636-2A=
ENST00000638452.2:c.1339-2A=	ENSP00000492349.2:n.1339-2A=
ENST00000638504.1:n.1322-2A=
ENST00000638568.2:c.1339-2A=	ENSP00000491158.2:n.1339-2A=
ENST00000639899.1:n.2155-2A=
ENST00000640655.2:c.1339-2A=	ENSP00000491596.2:n.1339-2A=
ENST00000651160.1:c.1636-2A=	ENSP00000498829.1:n.1636-2A=
ENST00000651541.1:c.1339-2A=	ENSP00000498795.1:n.1339-2A=
ENST00000651658.1:n.2063-2A=
ENST00000651723.1:c.*1719-2A=	ENSP00000498237.1:n.*1719-2A=
ENST00000652016.1:c.1636-2A=	ENSP00000498267.1:n.1636-2A=
ENST00000652485.1:c.1669-2A=	ENSP00000498973.1:n.1669-2A=
ENST00000378823.7:c.1636-2A=	ENSP00000368100.4:n.1636-2A=
ENST00000423956.5:c.1635+469A=	ENSP00000390971.1:n.1635+469A=
ENST00000434288.1:c.131-2A=
ENST00000453394.5:c.1453-2A=	ENSP00000400049.1:n.1453-2A=
ENST00000533482.5:c.*1262-2A=	ENSP00000431225.1:n.*1262-2A=
NM_005732.3:c.1636-2A=	NP_005723.2:n.1636-2A=
NM_005732.4:c.1636-2A= MANE Select	NP_005723.2:n.1636-2A=