Canonical Allele Identifier: CA127253465

Gene: RAD50

Linked Data

• dbSNP Id: rs983973565
• MyVariant Identifiers: chr5:g.131892628del (hg19) ; chr5:g.132556936del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132556939del , CM000667.2:g.132556939del	GRCh38
NC_000005.9:g.131892631del , CM000667.1:g.131892631del	GRCh37
NC_000005.8:g.131920530del	NCBI36
NG_021151.1:g.5016del
NG_021151.2:g.4963del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638452.2:c.-168-2345del	ENSP00000492349.2:n.-168-2345del
ENST00000638504.1:n.207-2345del
ENST00000638568.2:c.-169+466del	ENSP00000491158.2:n.-169+466del
ENST00000639899.1:n.290-2345del
ENST00000640655.2:c.-168-2345del	ENSP00000491596.2:n.-168-2345del
ENST00000651541.1:c.-239del	ENSP00000498795.1:n.-239del
ENST00000416135.5:c.-169+466del	ENSP00000389515.1:n.-169+466del
NM_005732.3:c.-386del	NP_005723.2:n.-386del