Canonical Allele Identifier: CA1583240546

Gene: RAD50

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132591824T= , CM000667.2:g.132591824T=	GRCh38
NC_000005.9:g.131927516T= , CM000667.1:g.131927516T=	GRCh37
NC_000005.8:g.131955415T=	NCBI36
NG_021151.1:g.39901T=
NG_021151.2:g.39848T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.1636-53T= MANE Select	ENSP00000368100.4:n.1636-53T=
ENST00000638452.2:c.1339-53T=	ENSP00000492349.2:n.1339-53T=
ENST00000638504.1:n.1322-53T=
ENST00000638568.2:c.1339-53T=	ENSP00000491158.2:n.1339-53T=
ENST00000639899.1:n.2155-53T=
ENST00000640655.2:c.1339-53T=	ENSP00000491596.2:n.1339-53T=
ENST00000651160.1:c.1636-53T=	ENSP00000498829.1:n.1636-53T=
ENST00000651541.1:c.1339-53T=	ENSP00000498795.1:n.1339-53T=
ENST00000651658.1:n.2063-53T=
ENST00000651723.1:c.*1719-53T=	ENSP00000498237.1:n.*1719-53T=
ENST00000652016.1:c.1636-53T=	ENSP00000498267.1:n.1636-53T=
ENST00000652485.1:c.1669-53T=	ENSP00000498973.1:n.1669-53T=
ENST00000378823.7:c.1636-53T=	ENSP00000368100.4:n.1636-53T=
ENST00000423956.5:c.1635+418T=	ENSP00000390971.1:n.1635+418T=
ENST00000434288.1:c.131-53T=
ENST00000453394.5:c.1453-53T=	ENSP00000400049.1:n.1453-53T=
ENST00000533482.5:c.*1262-53T=	ENSP00000431225.1:n.*1262-53T=
NM_005732.3:c.1636-53T=	NP_005723.2:n.1636-53T=
NM_005732.4:c.1636-53T= MANE Select	NP_005723.2:n.1636-53T=