Canonical Allele Identifier: CA127254018
Gene: RAD50 HGNC NCBI

Linked Data

dbSNP Id: rs186356727

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132557270C>T , CM000667.2:g.132557270C>T GRCh38
NC_000005.9:g.131892962C>T , CM000667.1:g.131892962C>T GRCh37
NC_000005.8:g.131920861C>T NCBI36
NG_021151.1:g.5347C>T
NG_021151.2:g.5294C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000378823.8:c.-55C>T MANE Select ENSP00000368100.4:n.-55C>T
ENST00000638452.2:c.-168-2014C>T ENSP00000492349.2:n.-168-2014C>T
ENST00000638504.1:n.207-2014C>T
ENST00000638568.2:c.-169+797C>T ENSP00000491158.2:n.-169+797C>T
ENST00000639899.1:n.290-2014C>T
ENST00000640655.2:c.-168-2014C>T ENSP00000491596.2:n.-168-2014C>T
ENST00000651160.1:c.-55C>T ENSP00000498829.1:n.-55C>T
ENST00000651541.1:c.-169+261C>T ENSP00000498795.1:n.-169+261C>T
ENST00000651658.1:n.14C>T
ENST00000651723.1:c.-55C>T ENSP00000498237.1:n.-55C>T
ENST00000652016.1:c.-55C>T ENSP00000498267.1:n.-55C>T
ENST00000652485.1:c.-55C>T ENSP00000498973.1:n.-55C>T
ENST00000378823.7:c.-55C>T ENSP00000368100.4:n.-55C>T
ENST00000416135.5:c.-169+797C>T ENSP00000389515.1:n.-169+797C>T
ENST00000423956.5:c.-55C>T ENSP00000390971.1:n.-55C>T
ENST00000453394.5:c.-55C>T ENSP00000400049.1:n.-55C>T
ENST00000533482.5:c.-55C>T ENSP00000431225.1:n.-55C>T
NM_005732.3:c.-55C>T NP_005723.2:n.-55C>T
NM_005732.4:c.-55C>T MANE Select NP_005723.2:n.-55C>T