Canonical Allele Identifier: CA360956434
Gene: RAD50 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132604863A>C , CM000667.2:g.132604863A>C GRCh38
NC_000005.9:g.131940555A>C , CM000667.1:g.131940555A>C GRCh37
NC_000005.8:g.131968454A>C NCBI36
NG_021151.1:g.52940A>C
NG_021151.2:g.52887A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378823.8:c.2582A>C MANE Select ENSP00000368100.4:p.Gln861Pro
ENST00000638452.2:c.2285A>C ENSP00000492349.2:p.Gln762Pro
ENST00000638504.1:n.2190A>C
ENST00000638568.2:c.2285A>C ENSP00000491158.2:p.Gln762Pro
ENST00000639899.1:n.3101A>C
ENST00000640655.2:c.2285A>C ENSP00000491596.2:p.Gln762Pro
ENST00000651160.1:c.*726A>C ENSP00000498829.1:n.*726A>C
ENST00000651723.1:c.*2665A>C ENSP00000498237.1:n.*2665A>C
ENST00000652016.1:c.*799A>C ENSP00000498267.1:n.*799A>C
ENST00000652485.1:c.2615A>C ENSP00000498973.1:p.Gln872Pro
ENST00000378823.7:c.2582A>C ENSP00000368100.4:p.Gln861Pro
ENST00000423956.5:c.*768A>C ENSP00000390971.1:n.*768A>C
ENST00000533482.5:c.*2208A>C ENSP00000431225.1:n.*2208A>C
NM_005732.3:c.2582A>C NP_005723.2:p.Gln861Pro
NM_005732.4:c.2582A>C MANE Select NP_005723.2:p.Gln861Pro