Canonical Allele Identifier: CA360948524

Gene: RAD50

Linked Data

• MyVariant Identifiers: chr5:g.131930715G>C (hg19) ; chr5:g.132595023G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132595023G>C , CM000667.2:g.132595023G>C	GRCh38
NC_000005.9:g.131930715G>C , CM000667.1:g.131930715G>C	GRCh37
NC_000005.8:g.131958614G>C	NCBI36
NG_021151.1:g.43100G>C
NG_021151.2:g.43047G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.1948G>C MANE Select	ENSP00000368100.4:p.Glu650Gln
ENST00000638452.2:c.1651G>C	ENSP00000492349.2:p.Glu551Gln
ENST00000638504.1:n.1480-81G>C
ENST00000638568.2:c.1651G>C	ENSP00000491158.2:p.Glu551Gln
ENST00000639899.1:n.2467G>C
ENST00000640655.2:c.1651G>C	ENSP00000491596.2:p.Glu551Gln
ENST00000651160.1:c.*16-81G>C	ENSP00000498829.1:n.*16-81G>C
ENST00000651658.1:n.2491G>C
ENST00000651723.1:c.*2031G>C	ENSP00000498237.1:n.*2031G>C
ENST00000652016.1:c.*89-81G>C	ENSP00000498267.1:n.*89-81G>C
ENST00000652485.1:c.1981G>C	ENSP00000498973.1:p.Glu661Gln
ENST00000378823.7:c.1948G>C	ENSP00000368100.4:p.Glu650Gln
ENST00000423956.5:c.*134G>C	ENSP00000390971.1:n.*134G>C
ENST00000453394.5:c.1765G>C	ENSP00000400049.1:p.Glu589Gln
ENST00000533482.5:c.*1574G>C	ENSP00000431225.1:n.*1574G>C
NM_005732.3:c.1948G>C	NP_005723.2:p.Glu650Gln
NM_005732.4:c.1948G>C MANE Select	NP_005723.2:p.Glu650Gln