Canonical Allele Identifier: CA360964738

Gene: RAD50

Linked Data

• dbSNP Id: rs2149853925
• MyVariant Identifiers: chr5:g.131953892G>A (hg19) ; chr5:g.132618200G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132618200G>A , CM000667.2:g.132618200G>A	GRCh38
NC_000005.9:g.131953892G>A , CM000667.1:g.131953892G>A	GRCh37
NC_000005.8:g.131981791G>A	NCBI36
NG_021151.1:g.66277G>A
NG_021151.2:g.66224G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.3295G>A MANE Select	ENSP00000368100.4:p.Asp1099Asn
ENST00000638452.2:c.2998G>A	ENSP00000492349.2:p.Asp1000Asn
ENST00000638504.1:n.2903G>A
ENST00000638568.2:c.2998G>A	ENSP00000491158.2:p.Asp1000Asn
ENST00000639899.1:n.3814G>A
ENST00000640655.2:c.2998G>A	ENSP00000491596.2:p.Asp1000Asn
ENST00000651249.1:c.131G>A
ENST00000378823.7:c.3295G>A	ENSP00000368100.4:p.Asp1099Asn
ENST00000533482.5:c.*2921G>A	ENSP00000431225.1:n.*2921G>A
NM_005732.3:c.3295G>A	NP_005723.2:p.Asp1099Asn
NM_005732.4:c.3295G>A MANE Select	NP_005723.2:p.Asp1099Asn