Canonical Allele Identifier: CA360935681

Gene: RAD50

Linked Data

• MyVariant Identifiers: chr5:g.131915592A>G (hg19) ; chr5:g.132579900A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132579900A>G , CM000667.2:g.132579900A>G	GRCh38
NC_000005.9:g.131915592A>G , CM000667.1:g.131915592A>G	GRCh37
NC_000005.8:g.131943491A>G	NCBI36
NG_021151.1:g.27977A>G
NG_021151.2:g.27924A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000378823.8:c.590A>G MANE Select	ENSP00000368100.4:p.Gln197Arg
ENST00000638452.2:c.293A>G	ENSP00000492349.2:p.Gln98Arg
ENST00000638504.1:n.442+3972A>G
ENST00000638568.2:c.293A>G	ENSP00000491158.2:p.Gln98Arg
ENST00000639899.1:n.1109A>G
ENST00000640655.2:c.293A>G	ENSP00000491596.2:p.Gln98Arg
ENST00000651160.1:c.590A>G	ENSP00000498829.1:p.Gln197Arg
ENST00000651541.1:c.293A>G	ENSP00000498795.1:p.Gln98Arg
ENST00000651658.1:n.1017A>G
ENST00000651723.1:c.*673A>G	ENSP00000498237.1:n.*673A>G
ENST00000652016.1:c.590A>G	ENSP00000498267.1:p.Gln197Arg
ENST00000652485.1:c.590A>G	ENSP00000498973.1:p.Gln197Arg
ENST00000378823.7:c.590A>G	ENSP00000368100.4:p.Gln197Arg
ENST00000416135.5:c.293A>G	ENSP00000389515.1:p.Gln98Arg
ENST00000423956.5:c.590A>G	ENSP00000390971.1:p.Gln197Arg
ENST00000453394.5:c.590A>G	ENSP00000400049.1:p.Gln197Arg
ENST00000487596.1:n.156A>G
ENST00000533482.5:c.*216A>G	ENSP00000431225.1:n.*216A>G
NM_005732.3:c.590A>G	NP_005723.2:p.Gln197Arg
NM_005732.4:c.590A>G MANE Select	NP_005723.2:p.Gln197Arg