Canonical Allele Identifier: CA446361955

Gene: RAD50

Linked Data

• MyVariant Identifiers: chr5:g.131930573T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132594881T>A , CM000667.2:g.132594881T>A	GRCh38
NC_000005.9:g.131930573T>A , CM000667.1:g.131930573T>A	GRCh37
NC_000005.8:g.131958472T>A	NCBI36
NG_021151.1:g.42958T>A
NG_021151.2:g.42905T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.1806T>A MANE Select	ENSP00000368100.4:p.Ala602=
ENST00000638452.2:c.1509T>A	ENSP00000492349.2:p.Ala503=
ENST00000638504.1:n.1480-223T>A
ENST00000638568.2:c.1509T>A	ENSP00000491158.2:p.Ala503=
ENST00000639899.1:n.2325T>A
ENST00000640655.2:c.1509T>A	ENSP00000491596.2:p.Ala503=
ENST00000651160.1:c.*16-223T>A	ENSP00000498829.1:n.*16-223T>A
ENST00000651658.1:n.2349T>A
ENST00000651723.1:c.*1889T>A	ENSP00000498237.1:n.*1889T>A
ENST00000652016.1:c.*88+204T>A	ENSP00000498267.1:n.*88+204T>A
ENST00000652485.1:c.1839T>A	ENSP00000498973.1:p.Ala613=
ENST00000378823.7:c.1806T>A	ENSP00000368100.4:p.Ala602=
ENST00000423956.5:c.1648T>A	ENSP00000390971.1:p.Phe550Ile
ENST00000453394.5:c.1623T>A	ENSP00000400049.1:p.Ala541=
ENST00000533482.5:c.*1432T>A	ENSP00000431225.1:n.*1432T>A
NM_005732.3:c.1806T>A	NP_005723.2:p.Ala602=
NM_005732.4:c.1806T>A MANE Select	NP_005723.2:p.Ala602=