Canonical Allele Identifier: CA360956905

Gene: RAD50

Linked Data

• MyVariant Identifiers: chr5:g.131940664A>C (hg19) ; chr5:g.132604972A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132604972A>C , CM000667.2:g.132604972A>C	GRCh38
NC_000005.9:g.131940664A>C , CM000667.1:g.131940664A>C	GRCh37
NC_000005.8:g.131968563A>C	NCBI36
NG_021151.1:g.53049A>C
NG_021151.2:g.52996A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.2691A>C MANE Select	ENSP00000368100.4:p.Glu897Asp
ENST00000638452.2:c.2394A>C	ENSP00000492349.2:p.Glu798Asp
ENST00000638504.1:n.2299A>C
ENST00000638568.2:c.2394A>C	ENSP00000491158.2:p.Glu798Asp
ENST00000639899.1:n.3210A>C
ENST00000640655.2:c.2394A>C	ENSP00000491596.2:p.Glu798Asp
ENST00000651160.1:c.*835A>C	ENSP00000498829.1:n.*835A>C
ENST00000651723.1:c.*2774A>C	ENSP00000498237.1:n.*2774A>C
ENST00000652016.1:c.*908A>C	ENSP00000498267.1:n.*908A>C
ENST00000378823.7:c.2691A>C	ENSP00000368100.4:p.Glu897Asp
ENST00000423956.5:c.*877A>C	ENSP00000390971.1:n.*877A>C
ENST00000533482.5:c.*2317A>C	ENSP00000431225.1:n.*2317A>C
NM_005732.3:c.2691A>C	NP_005723.2:p.Glu897Asp
NM_005732.4:c.2691A>C MANE Select	NP_005723.2:p.Glu897Asp