Canonical Allele Identifier: CA3405118

Gene: RAD50

Linked Data

• ClinVar Variation Id: 231300
• ClinVar RCV Id: RCV000219445
• dbSNP Id: rs139372231
• ExAC: 5:131924480 C / T
• gnomAD v2: 5-131924480-C-T
• gnomAD v3: 5-132588788-C-T
• gnomAD v4: 5-132588788-C-T
• MyVariant Identifiers: chr5:g.131924480C>T (hg19) ; chr5:g.132588788C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132588788C>T , CM000667.2:g.132588788C>T	GRCh38
NC_000005.9:g.131924480C>T , CM000667.1:g.131924480C>T	GRCh37
NC_000005.8:g.131952379C>T	NCBI36
NG_021151.1:g.36865C>T
NG_021151.2:g.36812C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.1153C>T MANE Select	ENSP00000368100.4:p.Arg385Cys
ENST00000638452.2:c.856C>T	ENSP00000492349.2:p.Arg286Cys
ENST00000638504.1:n.839C>T
ENST00000638568.2:c.856C>T	ENSP00000491158.2:p.Arg286Cys
ENST00000639899.1:n.1672C>T
ENST00000640655.2:c.856C>T	ENSP00000491596.2:p.Arg286Cys
ENST00000651160.1:c.1153C>T	ENSP00000498829.1:p.Arg385Cys
ENST00000651541.1:c.856C>T	ENSP00000498795.1:p.Arg286Cys
ENST00000651658.1:n.1580C>T
ENST00000651723.1:c.*1236C>T	ENSP00000498237.1:n.*1236C>T
ENST00000652016.1:c.1153C>T	ENSP00000498267.1:p.Arg385Cys
ENST00000652485.1:c.1153C>T	ENSP00000498973.1:p.Arg385Cys
ENST00000378823.7:c.1153C>T	ENSP00000368100.4:p.Arg385Cys
ENST00000423956.5:c.1153C>T	ENSP00000390971.1:p.Arg385Cys
ENST00000453394.5:c.1153C>T	ENSP00000400049.1:p.Arg385Cys
ENST00000487596.1:n.719C>T
ENST00000533482.5:c.*779C>T	ENSP00000431225.1:n.*779C>T
NM_005732.3:c.1153C>T	NP_005723.2:p.Arg385Cys
NM_005732.4:c.1153C>T MANE Select	NP_005723.2:p.Arg385Cys