Canonical Allele Identifier: CA1583233408
Gene: RAD50 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132617993A= , CM000667.2:g.132617993A= GRCh38
NC_000005.9:g.131953685A= , CM000667.1:g.131953685A= GRCh37
NC_000005.8:g.131981584A= NCBI36
NG_021151.1:g.66070A=
NG_021151.2:g.66017A=

Transcript Alleles

HGVS Amino-acid change
ENST00000378823.8:c.3165-77A= MANE Select ENSP00000368100.4:n.3165-77A=
ENST00000638452.2:c.2868-77A= ENSP00000492349.2:n.2868-77A=
ENST00000638504.1:n.2773-77A=
ENST00000638568.2:c.2868-77A= ENSP00000491158.2:n.2868-77A=
ENST00000639899.1:n.3684-77A=
ENST00000640655.2:c.2868-77A= ENSP00000491596.2:n.2868-77A=
ENST00000378823.7:c.3165-77A= ENSP00000368100.4:n.3165-77A=
ENST00000533482.5:c.*2791-77A= ENSP00000431225.1:n.*2791-77A=
NM_005732.3:c.3165-77A= NP_005723.2:n.3165-77A=
NM_005732.4:c.3165-77A= MANE Select NP_005723.2:n.3165-77A=