Canonical Allele Identifier: CA2675219036

Gene: RAD50

Linked Data

• gnomAD v4: 5-132617990-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132617993del , CM000667.2:g.132617993del	GRCh38
NC_000005.9:g.131953685del , CM000667.1:g.131953685del	GRCh37
NC_000005.8:g.131981584del	NCBI36
NG_021151.1:g.66070del
NG_021151.2:g.66017del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.3165-77del MANE Select	ENSP00000368100.4:n.3165-77del
ENST00000638452.2:c.2868-77del	ENSP00000492349.2:n.2868-77del
ENST00000638504.1:n.2773-77del
ENST00000638568.2:c.2868-77del	ENSP00000491158.2:n.2868-77del
ENST00000639899.1:n.3684-77del
ENST00000640655.2:c.2868-77del	ENSP00000491596.2:n.2868-77del
ENST00000378823.7:c.3165-77del	ENSP00000368100.4:n.3165-77del
ENST00000533482.5:c.*2791-77del	ENSP00000431225.1:n.*2791-77del
NM_005732.3:c.3165-77del	NP_005723.2:n.3165-77del
NM_005732.4:c.3165-77del MANE Select	NP_005723.2:n.3165-77del