Canonical Allele Identifier: CA360955490

Gene: RAD50

Linked Data

• MyVariant Identifiers: chr5:g.131939651G>T (hg19) ; chr5:g.132603959G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132603959G>T , CM000667.2:g.132603959G>T	GRCh38
NC_000005.9:g.131939651G>T , CM000667.1:g.131939651G>T	GRCh37
NC_000005.8:g.131967550G>T	NCBI36
NG_021151.1:g.52036G>T
NG_021151.2:g.51983G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.2437G>T MANE Select	ENSP00000368100.4:p.Ala813Ser
ENST00000638452.2:c.2140G>T	ENSP00000492349.2:p.Ala714Ser
ENST00000638504.1:n.2045G>T
ENST00000638568.2:c.2140G>T	ENSP00000491158.2:p.Ala714Ser
ENST00000639899.1:n.2956G>T
ENST00000640655.2:c.2140G>T	ENSP00000491596.2:p.Ala714Ser
ENST00000651160.1:c.*581G>T	ENSP00000498829.1:n.*581G>T
ENST00000651658.1:n.2980G>T
ENST00000651723.1:c.*2520G>T	ENSP00000498237.1:n.*2520G>T
ENST00000652016.1:c.*654G>T	ENSP00000498267.1:n.*654G>T
ENST00000652485.1:c.2470G>T	ENSP00000498973.1:p.Ala824Ser
ENST00000378823.7:c.2437G>T	ENSP00000368100.4:p.Ala813Ser
ENST00000423956.5:c.*623G>T	ENSP00000390971.1:n.*623G>T
ENST00000533482.5:c.*2063G>T	ENSP00000431225.1:n.*2063G>T
NM_005732.3:c.2437G>T	NP_005723.2:p.Ala813Ser
NM_005732.4:c.2437G>T MANE Select	NP_005723.2:p.Ala813Ser