Canonical Allele Identifier: CA1583229627

Gene: RAD50

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132609255T= , CM000667.2:g.132609255T=	GRCh38
NC_000005.9:g.131944947T= , CM000667.1:g.131944947T=	GRCh37
NC_000005.8:g.131972846T=	NCBI36
NG_021151.1:g.57332T=
NG_021151.2:g.57279T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000378823.8:c.2923-28T= MANE Select	ENSP00000368100.4:n.2923-28T=
ENST00000638452.2:c.2626-28T=	ENSP00000492349.2:n.2626-28T=
ENST00000638504.1:n.2531-28T=
ENST00000638568.2:c.2626-28T=	ENSP00000491158.2:n.2626-28T=
ENST00000639899.1:n.3442-28T=
ENST00000640655.2:c.2626-28T=	ENSP00000491596.2:n.2626-28T=
ENST00000651160.1:c.*1067-28T=	ENSP00000498829.1:n.*1067-28T=
ENST00000651723.1:c.*3006-28T=	ENSP00000498237.1:n.*3006-28T=
ENST00000378823.7:c.2923-28T=	ENSP00000368100.4:n.2923-28T=
ENST00000423956.5:c.*1109-28T=	ENSP00000390971.1:n.*1109-28T=
ENST00000533482.5:c.*2549-28T=	ENSP00000431225.1:n.*2549-28T=
NM_005732.3:c.2923-28T=	NP_005723.2:n.2923-28T=
NM_005732.4:c.2923-28T= MANE Select	NP_005723.2:n.2923-28T=