Canonical Allele Identifier: CA360947570

Gene: RAD50

Linked Data

• MyVariant Identifiers: chr5:g.131930595C>T (hg19) ; chr5:g.132594903C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132594903C>T , CM000667.2:g.132594903C>T	GRCh38
NC_000005.9:g.131930595C>T , CM000667.1:g.131930595C>T	GRCh37
NC_000005.8:g.131958494C>T	NCBI36
NG_021151.1:g.42980C>T
NG_021151.2:g.42927C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.1828C>T MANE Select	ENSP00000368100.4:p.His610Tyr
ENST00000638452.2:c.1531C>T	ENSP00000492349.2:p.His511Tyr
ENST00000638504.1:n.1480-201C>T
ENST00000638568.2:c.1531C>T	ENSP00000491158.2:p.His511Tyr
ENST00000639899.1:n.2347C>T
ENST00000640655.2:c.1531C>T	ENSP00000491596.2:p.His511Tyr
ENST00000651160.1:c.*16-201C>T	ENSP00000498829.1:n.*16-201C>T
ENST00000651658.1:n.2371C>T
ENST00000651723.1:c.*1911C>T	ENSP00000498237.1:n.*1911C>T
ENST00000652016.1:c.*89-201C>T	ENSP00000498267.1:n.*89-201C>T
ENST00000652485.1:c.1861C>T	ENSP00000498973.1:p.His621Tyr
ENST00000378823.7:c.1828C>T	ENSP00000368100.4:p.His610Tyr
ENST00000423956.5:c.*14C>T	ENSP00000390971.1:n.*14C>T
ENST00000453394.5:c.1645C>T	ENSP00000400049.1:p.His549Tyr
ENST00000533482.5:c.*1454C>T	ENSP00000431225.1:n.*1454C>T
NM_005732.3:c.1828C>T	NP_005723.2:p.His610Tyr
NM_005732.4:c.1828C>T MANE Select	NP_005723.2:p.His610Tyr