Canonical Allele Identifier: CA10578574

Gene: RAD50

Linked Data

• ClinVar Variation Id: 232201
• ClinVar RCV Id: RCV000230454
• dbSNP Id: rs876659612
• MyVariant Identifiers: chr5:g.131940678A>C (hg19) ; chr5:g.132604986A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132604986A>C , CM000667.2:g.132604986A>C	GRCh38
NC_000005.9:g.131940678A>C , CM000667.1:g.131940678A>C	GRCh37
NC_000005.8:g.131968577A>C	NCBI36
NG_021151.1:g.53063A>C
NG_021151.2:g.53010A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.2705A>C MANE Select	ENSP00000368100.4:p.Tyr902Ser
ENST00000638452.2:c.2408A>C	ENSP00000492349.2:p.Tyr803Ser
ENST00000638504.1:n.2313A>C
ENST00000638568.2:c.2408A>C	ENSP00000491158.2:p.Tyr803Ser
ENST00000639899.1:n.3224A>C
ENST00000640655.2:c.2408A>C	ENSP00000491596.2:p.Tyr803Ser
ENST00000651160.1:c.*849A>C	ENSP00000498829.1:n.*849A>C
ENST00000651723.1:c.*2788A>C	ENSP00000498237.1:n.*2788A>C
ENST00000652016.1:c.*922A>C	ENSP00000498267.1:n.*922A>C
ENST00000378823.7:c.2705A>C	ENSP00000368100.4:p.Tyr902Ser
ENST00000423956.5:c.*891A>C	ENSP00000390971.1:n.*891A>C
ENST00000533482.5:c.*2331A>C	ENSP00000431225.1:n.*2331A>C
NM_005732.3:c.2705A>C	NP_005723.2:p.Tyr902Ser
NM_005732.4:c.2705A>C MANE Select	NP_005723.2:p.Tyr902Ser