Canonical Allele Identifier: CA360961085

Gene: RAD50

Linked Data

• ClinVar Variation Id: 657690
• ClinVar RCV Id: RCV000814353
• dbSNP Id: rs1581004991
• gnomAD v4: 5-132609389-C-T
• MyVariant Identifiers: chr5:g.131945081C>T (hg19) ; chr5:g.132609389C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132609389C>T , CM000667.2:g.132609389C>T	GRCh38
NC_000005.9:g.131945081C>T , CM000667.1:g.131945081C>T	GRCh37
NC_000005.8:g.131972980C>T	NCBI36
NG_021151.1:g.57466C>T
NG_021151.2:g.57413C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000378823.8:c.3029C>T MANE Select	ENSP00000368100.4:p.Thr1010Ile
ENST00000638452.2:c.2732C>T	ENSP00000492349.2:p.Thr911Ile
ENST00000638504.1:n.2637C>T
ENST00000638568.2:c.2732C>T	ENSP00000491158.2:p.Thr911Ile
ENST00000639899.1:n.3548C>T
ENST00000640655.2:c.2732C>T	ENSP00000491596.2:p.Thr911Ile
ENST00000651723.1:c.*3112C>T	ENSP00000498237.1:n.*3112C>T
ENST00000378823.7:c.3029C>T	ENSP00000368100.4:p.Thr1010Ile
ENST00000533482.5:c.*2655C>T	ENSP00000431225.1:n.*2655C>T
NM_005732.3:c.3029C>T	NP_005723.2:p.Thr1010Ile
NM_005732.4:c.3029C>T MANE Select	NP_005723.2:p.Thr1010Ile