Canonical Allele Identifier: CA1583252442

Gene: RAD50 TH2LCRR

Linked Data

• dbSNP Id: rs1751607678

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132637395G>A , CM000667.2:g.132637395G>A	GRCh38
NC_000005.9:g.131973087G>A , CM000667.1:g.131973087G>A	GRCh37
NC_000005.8:g.132000986G>A	NCBI36
NG_021151.1:g.85472G>A
NG_021151.2:g.85419G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.3475+195G>A (RAD50) MANE Select	ENSP00000368100.4:n.3475+195G>A
ENST00000638452.2:c.3178+195G>A	ENSP00000492349.2:n.3178+195G>A
ENST00000638504.1:n.3083+195G>A
ENST00000638568.2:c.3178+195G>A	ENSP00000491158.2:n.3178+195G>A
ENST00000639899.1:n.3994+195G>A
ENST00000640655.2:c.3178+195G>A	ENSP00000491596.2:n.3178+195G>A
ENST00000651249.1:c.311+195G>A (RAD50)
ENST00000378823.7:c.3475+195G>A (RAD50)	ENSP00000368100.4:n.3475+195G>A
ENST00000455677.1:c.110+195G>A (RAD50)
ENST00000533482.5:c.*3101+195G>A (RAD50)	ENSP00000431225.1:n.*3101+195G>A
NM_005732.3:c.3475+195G>A (RAD50)	NP_005723.2:n.3475+195G>A
NR_132124.1:n.153+763C>T (TH2LCRR)
NM_005732.4:c.3475+195G>A (RAD50) MANE Select	NP_005723.2:n.3475+195G>A