Canonical Allele Identifier: CA446364829

Gene: RAD50

Linked Data

• MyVariant Identifiers: chr5:g.131953828A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132618136A>T , CM000667.2:g.132618136A>T	GRCh38
NC_000005.9:g.131953828A>T , CM000667.1:g.131953828A>T	GRCh37
NC_000005.8:g.131981727A>T	NCBI36
NG_021151.1:g.66213A>T
NG_021151.2:g.66160A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.3231A>T MANE Select	ENSP00000368100.4:p.Arg1077=
ENST00000638452.2:c.2934A>T	ENSP00000492349.2:p.Arg978=
ENST00000638504.1:n.2839A>T
ENST00000638568.2:c.2934A>T	ENSP00000491158.2:p.Arg978=
ENST00000639899.1:n.3750A>T
ENST00000640655.2:c.2934A>T	ENSP00000491596.2:p.Arg978=
ENST00000651249.1:c.67A>T
ENST00000378823.7:c.3231A>T	ENSP00000368100.4:p.Arg1077=
ENST00000533482.5:c.*2857A>T	ENSP00000431225.1:n.*2857A>T
NM_005732.3:c.3231A>T	NP_005723.2:p.Arg1077=
NM_005732.4:c.3231A>T MANE Select	NP_005723.2:p.Arg1077=