Canonical Allele Identifier: CA1583225155

Gene: RAD50

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132575678G= , CM000667.2:g.132575678G=	GRCh38
NC_000005.9:g.131911370G= , CM000667.1:g.131911370G=	GRCh37
NC_000005.8:g.131939269G=	NCBI36
NG_021151.1:g.23755G=
NG_021151.2:g.23702G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.214-99G= MANE Select	ENSP00000368100.4:n.214-99G=
ENST00000638452.2:c.-84-99G=	ENSP00000492349.2:n.-84-99G=
ENST00000638504.1:n.291-99G=
ENST00000638568.2:c.-84-99G=	ENSP00000491158.2:n.-84-99G=
ENST00000639899.1:n.374-99G=
ENST00000640655.2:c.-84-99G=	ENSP00000491596.2:n.-84-99G=
ENST00000651160.1:c.214-99G=	ENSP00000498829.1:n.214-99G=
ENST00000651541.1:c.-84-99G=	ENSP00000498795.1:n.-84-99G=
ENST00000651658.1:n.282-99G=
ENST00000651723.1:c.*362-99G=	ENSP00000498237.1:n.*362-99G=
ENST00000652016.1:c.214-99G=	ENSP00000498267.1:n.214-99G=
ENST00000652485.1:c.214-99G=	ENSP00000498973.1:n.214-99G=
ENST00000378823.7:c.214-99G=	ENSP00000368100.4:n.214-99G=
ENST00000416135.5:c.-84-99G=	ENSP00000389515.1:n.-84-99G=
ENST00000423956.5:c.214-99G=	ENSP00000390971.1:n.214-99G=
ENST00000453394.5:c.214-99G=	ENSP00000400049.1:n.214-99G=
ENST00000533482.5:c.214-99G=	ENSP00000431225.1:n.214-99G=
NM_005732.3:c.214-99G=	NP_005723.2:n.214-99G=
NM_005732.4:c.214-99G= MANE Select	NP_005723.2:n.214-99G=