Canonical Allele Identifier: CA360959793

Gene: RAD50

Linked Data

• MyVariant Identifiers: chr5:g.131944867A>T (hg19) ; chr5:g.132609175A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132609175A>T , CM000667.2:g.132609175A>T	GRCh38
NC_000005.9:g.131944867A>T , CM000667.1:g.131944867A>T	GRCh37
NC_000005.8:g.131972766A>T	NCBI36
NG_021151.1:g.57252A>T
NG_021151.2:g.57199A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000378823.8:c.2888A>T MANE Select	ENSP00000368100.4:p.Asn963Ile
ENST00000638452.2:c.2591A>T	ENSP00000492349.2:p.Asn864Ile
ENST00000638504.1:n.2496A>T
ENST00000638568.2:c.2591A>T	ENSP00000491158.2:p.Asn864Ile
ENST00000639899.1:n.3407A>T
ENST00000640655.2:c.2591A>T	ENSP00000491596.2:p.Asn864Ile
ENST00000651160.1:c.*1032A>T	ENSP00000498829.1:n.*1032A>T
ENST00000651723.1:c.*2971A>T	ENSP00000498237.1:n.*2971A>T
ENST00000378823.7:c.2888A>T	ENSP00000368100.4:p.Asn963Ile
ENST00000423956.5:c.*1074A>T	ENSP00000390971.1:n.*1074A>T
ENST00000533482.5:c.*2514A>T	ENSP00000431225.1:n.*2514A>T
NM_005732.3:c.2888A>T	NP_005723.2:p.Asn963Ile
NM_005732.4:c.2888A>T MANE Select	NP_005723.2:p.Asn963Ile