Canonical Allele Identifier: CA360960787

Gene: RAD50

Linked Data

• MyVariant Identifiers: chr5:g.131945046T>G (hg19) ; chr5:g.132609354T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132609354T>G , CM000667.2:g.132609354T>G	GRCh38
NC_000005.9:g.131945046T>G , CM000667.1:g.131945046T>G	GRCh37
NC_000005.8:g.131972945T>G	NCBI36
NG_021151.1:g.57431T>G
NG_021151.2:g.57378T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.2994T>G MANE Select	ENSP00000368100.4:p.Asn998Lys
ENST00000638452.2:c.2697T>G	ENSP00000492349.2:p.Asn899Lys
ENST00000638504.1:n.2602T>G
ENST00000638568.2:c.2697T>G	ENSP00000491158.2:p.Asn899Lys
ENST00000639899.1:n.3513T>G
ENST00000640655.2:c.2697T>G	ENSP00000491596.2:p.Asn899Lys
ENST00000651723.1:c.*3077T>G	ENSP00000498237.1:n.*3077T>G
ENST00000378823.7:c.2994T>G	ENSP00000368100.4:p.Asn998Lys
ENST00000533482.5:c.*2620T>G	ENSP00000431225.1:n.*2620T>G
NM_005732.3:c.2994T>G	NP_005723.2:p.Asn998Lys
NM_005732.4:c.2994T>G MANE Select	NP_005723.2:p.Asn998Lys