Canonical Allele Identifier: CA1583229620
Gene: RAD50 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132609250A= , CM000667.2:g.132609250A= GRCh38
NC_000005.9:g.131944942A= , CM000667.1:g.131944942A= GRCh37
NC_000005.8:g.131972841A= NCBI36
NG_021151.1:g.57327A=
NG_021151.2:g.57274A=

Transcript Alleles

HGVS Amino-acid change
ENST00000378823.8:c.2923-33A= MANE Select ENSP00000368100.4:n.2923-33A=
ENST00000638452.2:c.2626-33A= ENSP00000492349.2:n.2626-33A=
ENST00000638504.1:n.2531-33A=
ENST00000638568.2:c.2626-33A= ENSP00000491158.2:n.2626-33A=
ENST00000639899.1:n.3442-33A=
ENST00000640655.2:c.2626-33A= ENSP00000491596.2:n.2626-33A=
ENST00000651160.1:c.*1067-33A= ENSP00000498829.1:n.*1067-33A=
ENST00000651723.1:c.*3006-33A= ENSP00000498237.1:n.*3006-33A=
ENST00000378823.7:c.2923-33A= ENSP00000368100.4:n.2923-33A=
ENST00000423956.5:c.*1109-33A= ENSP00000390971.1:n.*1109-33A=
ENST00000533482.5:c.*2549-33A= ENSP00000431225.1:n.*2549-33A=
NM_005732.3:c.2923-33A= NP_005723.2:n.2923-33A=
NM_005732.4:c.2923-33A= MANE Select NP_005723.2:n.2923-33A=