Canonical Allele Identifier: CA1583216703
Gene: RAD50 HGNC NCBI

Linked Data

dbSNP Id: rs1750001567

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132556971_132556972del , CM000667.2:g.132556971_132556972del GRCh38
NC_000005.9:g.131892663_131892664del , CM000667.1:g.131892663_131892664del GRCh37
NC_000005.8:g.131920562_131920563del NCBI36
NG_021151.1:g.5048_5049del
NG_021151.2:g.4995_4996del

Transcript Alleles

HGVS Amino-acid Change
ENST00000638452.2:c.-168-2313_-168-2312del ENSP00000492349.2:n.-168-2313_-168-2312del
ENST00000638504.1:n.207-2313_207-2312del
ENST00000638568.2:c.-169+498_-169+499del ENSP00000491158.2:n.-169+498_-169+499del
ENST00000639899.1:n.290-2313_290-2312del
ENST00000640655.2:c.-168-2313_-168-2312del ENSP00000491596.2:n.-168-2313_-168-2312del
ENST00000651541.1:c.-207_-206del ENSP00000498795.1:n.-207_-206del
ENST00000378823.7:c.-354_-353del ENSP00000368100.4:n.-354_-353del
ENST00000416135.5:c.-169+498_-169+499del ENSP00000389515.1:n.-169+498_-169+499del
ENST00000533482.5:c.-354_-353del ENSP00000431225.1:n.-354_-353del
NM_005732.3:c.-354_-353del NP_005723.2:n.-354_-353del