Canonical Allele Identifier: CA1583216699
Gene: RAD50 HGNC NCBI

Linked Data

dbSNP Id: rs1750001389

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132556967dup , CM000667.2:g.132556967dup GRCh38
NC_000005.9:g.131892659dup , CM000667.1:g.131892659dup GRCh37
NC_000005.8:g.131920558dup NCBI36
NG_021151.1:g.5044dup
NG_021151.2:g.4991dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000638452.2:c.-168-2317dup ENSP00000492349.2:n.-168-2317dup
ENST00000638504.1:n.207-2317dup
ENST00000638568.2:c.-169+494dup ENSP00000491158.2:n.-169+494dup
ENST00000639899.1:n.290-2317dup
ENST00000640655.2:c.-168-2317dup ENSP00000491596.2:n.-168-2317dup
ENST00000651541.1:c.-211dup ENSP00000498795.1:n.-211dup
ENST00000378823.7:c.-358dup ENSP00000368100.4:n.-358dup
ENST00000416135.5:c.-169+494dup ENSP00000389515.1:n.-169+494dup
ENST00000533482.5:c.-358dup ENSP00000431225.1:n.-358dup
NM_005732.3:c.-358dup NP_005723.2:n.-358dup