Canonical Allele Identifier: CA360948606

Gene: RAD50

Linked Data

• MyVariant Identifiers: chr5:g.131930725C>G (hg19) ; chr5:g.132595033C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132595033C>G , CM000667.2:g.132595033C>G	GRCh38
NC_000005.9:g.131930725C>G , CM000667.1:g.131930725C>G	GRCh37
NC_000005.8:g.131958624C>G	NCBI36
NG_021151.1:g.43110C>G
NG_021151.2:g.43057C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.1958C>G MANE Select	ENSP00000368100.4:p.Ser653Ter
ENST00000638452.2:c.1661C>G	ENSP00000492349.2:p.Ser554Ter
ENST00000638504.1:n.1480-71C>G
ENST00000638568.2:c.1661C>G	ENSP00000491158.2:p.Ser554Ter
ENST00000639899.1:n.2477C>G
ENST00000640655.2:c.1661C>G	ENSP00000491596.2:p.Ser554Ter
ENST00000651160.1:c.*16-71C>G	ENSP00000498829.1:n.*16-71C>G
ENST00000651658.1:n.2501C>G
ENST00000651723.1:c.*2041C>G	ENSP00000498237.1:n.*2041C>G
ENST00000652016.1:c.*89-71C>G	ENSP00000498267.1:n.*89-71C>G
ENST00000652485.1:c.1991C>G	ENSP00000498973.1:p.Ser664Ter
ENST00000378823.7:c.1958C>G	ENSP00000368100.4:p.Ser653Ter
ENST00000423956.5:c.*144C>G	ENSP00000390971.1:n.*144C>G
ENST00000453394.5:c.1775C>G	ENSP00000400049.1:p.Ser592Ter
ENST00000533482.5:c.*1584C>G	ENSP00000431225.1:n.*1584C>G
NM_005732.3:c.1958C>G	NP_005723.2:p.Ser653Ter
NM_005732.4:c.1958C>G MANE Select	NP_005723.2:p.Ser653Ter