Canonical Allele Identifier: CA446364881

Gene: RAD50

Linked Data

• MyVariant Identifiers: chr5:g.131953873T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132618181T>G , CM000667.2:g.132618181T>G	GRCh38
NC_000005.9:g.131953873T>G , CM000667.1:g.131953873T>G	GRCh37
NC_000005.8:g.131981772T>G	NCBI36
NG_021151.1:g.66258T>G
NG_021151.2:g.66205T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000378823.8:c.3276T>G MANE Select	ENSP00000368100.4:p.Leu1092=
ENST00000638452.2:c.2979T>G	ENSP00000492349.2:p.Leu993=
ENST00000638504.1:n.2884T>G
ENST00000638568.2:c.2979T>G	ENSP00000491158.2:p.Leu993=
ENST00000639899.1:n.3795T>G
ENST00000640655.2:c.2979T>G	ENSP00000491596.2:p.Leu993=
ENST00000651249.1:c.112T>G
ENST00000378823.7:c.3276T>G	ENSP00000368100.4:p.Leu1092=
ENST00000533482.5:c.*2902T>G	ENSP00000431225.1:n.*2902T>G
NM_005732.3:c.3276T>G	NP_005723.2:p.Leu1092=
NM_005732.4:c.3276T>G MANE Select	NP_005723.2:p.Leu1092=