Canonical Allele Identifier: CA360964260

Gene: RAD50

Linked Data

• MyVariant Identifiers: chr5:g.131953785A>G (hg19) ; chr5:g.132618093A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132618093A>G , CM000667.2:g.132618093A>G	GRCh38
NC_000005.9:g.131953785A>G , CM000667.1:g.131953785A>G	GRCh37
NC_000005.8:g.131981684A>G	NCBI36
NG_021151.1:g.66170A>G
NG_021151.2:g.66117A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000378823.8:c.3188A>G MANE Select	ENSP00000368100.4:p.Asn1063Ser
ENST00000638452.2:c.2891A>G	ENSP00000492349.2:p.Asn964Ser
ENST00000638504.1:n.2796A>G
ENST00000638568.2:c.2891A>G	ENSP00000491158.2:p.Asn964Ser
ENST00000639899.1:n.3707A>G
ENST00000640655.2:c.2891A>G	ENSP00000491596.2:p.Asn964Ser
ENST00000651249.1:c.24A>G
ENST00000378823.7:c.3188A>G	ENSP00000368100.4:p.Asn1063Ser
ENST00000533482.5:c.*2814A>G	ENSP00000431225.1:n.*2814A>G
NM_005732.3:c.3188A>G	NP_005723.2:p.Asn1063Ser
NM_005732.4:c.3188A>G MANE Select	NP_005723.2:p.Asn1063Ser