Canonical Allele Identifier: CA360947493

Gene: RAD50

Linked Data

• MyVariant Identifiers: chr5:g.131930585G>C (hg19) ; chr5:g.132594893G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132594893G>C , CM000667.2:g.132594893G>C	GRCh38
NC_000005.9:g.131930585G>C , CM000667.1:g.131930585G>C	GRCh37
NC_000005.8:g.131958484G>C	NCBI36
NG_021151.1:g.42970G>C
NG_021151.2:g.42917G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.1818G>C MANE Select	ENSP00000368100.4:p.Gln606His
ENST00000638452.2:c.1521G>C	ENSP00000492349.2:p.Gln507His
ENST00000638504.1:n.1480-211G>C
ENST00000638568.2:c.1521G>C	ENSP00000491158.2:p.Gln507His
ENST00000639899.1:n.2337G>C
ENST00000640655.2:c.1521G>C	ENSP00000491596.2:p.Gln507His
ENST00000651160.1:c.*16-211G>C	ENSP00000498829.1:n.*16-211G>C
ENST00000651658.1:n.2361G>C
ENST00000651723.1:c.*1901G>C	ENSP00000498237.1:n.*1901G>C
ENST00000652016.1:c.*89-211G>C	ENSP00000498267.1:n.*89-211G>C
ENST00000652485.1:c.1851G>C	ENSP00000498973.1:p.Gln617His
ENST00000378823.7:c.1818G>C	ENSP00000368100.4:p.Gln606His
ENST00000423956.5:c.*4G>C	ENSP00000390971.1:n.*4G>C
ENST00000453394.5:c.1635G>C	ENSP00000400049.1:p.Gln545His
ENST00000533482.5:c.*1444G>C	ENSP00000431225.1:n.*1444G>C
NM_005732.3:c.1818G>C	NP_005723.2:p.Gln606His
NM_005732.4:c.1818G>C MANE Select	NP_005723.2:p.Gln606His