Canonical Allele Identifier: CA360947954

Gene: RAD50

Linked Data

• MyVariant Identifiers: chr5:g.131930646G>T (hg19) ; chr5:g.132594954G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132594954G>T , CM000667.2:g.132594954G>T	GRCh38
NC_000005.9:g.131930646G>T , CM000667.1:g.131930646G>T	GRCh37
NC_000005.8:g.131958545G>T	NCBI36
NG_021151.1:g.43031G>T
NG_021151.2:g.42978G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.1879G>T MANE Select	ENSP00000368100.4:p.Asp627Tyr
ENST00000638452.2:c.1582G>T	ENSP00000492349.2:p.Asp528Tyr
ENST00000638504.1:n.1480-150G>T
ENST00000638568.2:c.1582G>T	ENSP00000491158.2:p.Asp528Tyr
ENST00000639899.1:n.2398G>T
ENST00000640655.2:c.1582G>T	ENSP00000491596.2:p.Asp528Tyr
ENST00000651160.1:c.*16-150G>T	ENSP00000498829.1:n.*16-150G>T
ENST00000651658.1:n.2422G>T
ENST00000651723.1:c.*1962G>T	ENSP00000498237.1:n.*1962G>T
ENST00000652016.1:c.*89-150G>T	ENSP00000498267.1:n.*89-150G>T
ENST00000652485.1:c.1912G>T	ENSP00000498973.1:p.Asp638Tyr
ENST00000378823.7:c.1879G>T	ENSP00000368100.4:p.Asp627Tyr
ENST00000423956.5:c.*65G>T	ENSP00000390971.1:n.*65G>T
ENST00000453394.5:c.1696G>T	ENSP00000400049.1:p.Asp566Tyr
ENST00000533482.5:c.*1505G>T	ENSP00000431225.1:n.*1505G>T
NM_005732.3:c.1879G>T	NP_005723.2:p.Asp627Tyr
NM_005732.4:c.1879G>T MANE Select	NP_005723.2:p.Asp627Tyr