Canonical Allele Identifier: CA1583229551

Gene: RAD50

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132609138G= , CM000667.2:g.132609138G=	GRCh38
NC_000005.9:g.131944830G= , CM000667.1:g.131944830G=	GRCh37
NC_000005.8:g.131972729G=	NCBI36
NG_021151.1:g.57215G=
NG_021151.2:g.57162G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.2851G= MANE Select	ENSP00000368100.4:p.Val951=
ENST00000638452.2:c.2554G=	ENSP00000492349.2:p.Val852=
ENST00000638504.1:n.2459G=
ENST00000638568.2:c.2554G=	ENSP00000491158.2:p.Val852=
ENST00000639899.1:n.3370G=
ENST00000640655.2:c.2554G=	ENSP00000491596.2:p.Val852=
ENST00000651160.1:c.*995G=	ENSP00000498829.1:n.*995G=
ENST00000651723.1:c.*2934G=	ENSP00000498237.1:n.*2934G=
ENST00000378823.7:c.2851G=	ENSP00000368100.4:p.Val951=
ENST00000423956.5:c.*1037G=	ENSP00000390971.1:n.*1037G=
ENST00000533482.5:c.*2477G=	ENSP00000431225.1:n.*2477G=
NM_005732.3:c.2851G=	NP_005723.2:p.Val951=
NM_005732.4:c.2851G= MANE Select	NP_005723.2:p.Val951=