Canonical Allele Identifier: CA127260868

Gene: RAD50

Linked Data

• dbSNP Id: rs1554099377
• MyVariant Identifiers: chr5:g.131944963_131944964insT (hg19) ; chr5:g.132609271_132609272insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132609271dup , CM000667.2:g.132609271dup	GRCh38
NC_000005.9:g.131944963dup , CM000667.1:g.131944963dup	GRCh37
NC_000005.8:g.131972862dup	NCBI36
NG_021151.1:g.57348dup
NG_021151.2:g.57295dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000378823.8:c.2923-12dup MANE Select	ENSP00000368100.4:n.2923-12dup
ENST00000638452.2:c.2626-12dup	ENSP00000492349.2:n.2626-12dup
ENST00000638504.1:n.2531-12dup
ENST00000638568.2:c.2626-12dup	ENSP00000491158.2:n.2626-12dup
ENST00000639899.1:n.3442-12dup
ENST00000640655.2:c.2626-12dup	ENSP00000491596.2:n.2626-12dup
ENST00000651160.1:c.*1067-12dup	ENSP00000498829.1:n.*1067-12dup
ENST00000651723.1:c.*3006-12dup	ENSP00000498237.1:n.*3006-12dup
ENST00000378823.7:c.2923-12dup	ENSP00000368100.4:n.2923-12dup
ENST00000423956.5:c.*1109-12dup	ENSP00000390971.1:n.*1109-12dup
ENST00000533482.5:c.*2549-12dup	ENSP00000431225.1:n.*2549-12dup
NM_005732.3:c.2923-12dup	NP_005723.2:n.2923-12dup
NM_005732.4:c.2923-12dup MANE Select	NP_005723.2:n.2923-12dup