Canonical Allele Identifier: CA360949290

Gene: RAD50

Linked Data

• MyVariant Identifiers: chr5:g.131931291T>G (hg19) ; chr5:g.132595599T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132595599T>G , CM000667.2:g.132595599T>G	GRCh38
NC_000005.9:g.131931291T>G , CM000667.1:g.131931291T>G	GRCh37
NC_000005.8:g.131959190T>G	NCBI36
NG_021151.1:g.43676T>G
NG_021151.2:g.43623T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.1996T>G MANE Select	ENSP00000368100.4:p.Tyr666Asp
ENST00000638452.2:c.1699T>G	ENSP00000492349.2:p.Tyr567Asp
ENST00000638504.1:n.1604T>G
ENST00000638568.2:c.1699T>G	ENSP00000491158.2:p.Tyr567Asp
ENST00000639899.1:n.2515T>G
ENST00000640655.2:c.1699T>G	ENSP00000491596.2:p.Tyr567Asp
ENST00000651160.1:c.*140T>G	ENSP00000498829.1:n.*140T>G
ENST00000651658.1:n.2539T>G
ENST00000651723.1:c.*2079T>G	ENSP00000498237.1:n.*2079T>G
ENST00000652016.1:c.*213T>G	ENSP00000498267.1:n.*213T>G
ENST00000652485.1:c.2029T>G	ENSP00000498973.1:p.Tyr677Asp
ENST00000378823.7:c.1996T>G	ENSP00000368100.4:p.Tyr666Asp
ENST00000423956.5:c.*182T>G	ENSP00000390971.1:n.*182T>G
ENST00000453394.5:c.1813T>G	ENSP00000400049.1:p.Tyr605Asp
ENST00000496204.1:n.79T>G
ENST00000533482.5:c.*1622T>G	ENSP00000431225.1:n.*1622T>G
NM_005732.3:c.1996T>G	NP_005723.2:p.Tyr666Asp
NM_005732.4:c.1996T>G MANE Select	NP_005723.2:p.Tyr666Asp