Canonical Allele Identifier: CA360961100

Gene: RAD50

Linked Data

• MyVariant Identifiers: chr5:g.131945083C>G (hg19) ; chr5:g.132609391C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132609391C>G , CM000667.2:g.132609391C>G	GRCh38
NC_000005.9:g.131945083C>G , CM000667.1:g.131945083C>G	GRCh37
NC_000005.8:g.131972982C>G	NCBI36
NG_021151.1:g.57468C>G
NG_021151.2:g.57415C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000378823.8:c.3031C>G MANE Select	ENSP00000368100.4:p.Gln1011Glu
ENST00000638452.2:c.2734C>G	ENSP00000492349.2:p.Gln912Glu
ENST00000638504.1:n.2639C>G
ENST00000638568.2:c.2734C>G	ENSP00000491158.2:p.Gln912Glu
ENST00000639899.1:n.3550C>G
ENST00000640655.2:c.2734C>G	ENSP00000491596.2:p.Gln912Glu
ENST00000651723.1:c.*3114C>G	ENSP00000498237.1:n.*3114C>G
ENST00000378823.7:c.3031C>G	ENSP00000368100.4:p.Gln1011Glu
ENST00000533482.5:c.*2657C>G	ENSP00000431225.1:n.*2657C>G
NM_005732.3:c.3031C>G	NP_005723.2:p.Gln1011Glu
NM_005732.4:c.3031C>G MANE Select	NP_005723.2:p.Gln1011Glu