Canonical Allele Identifier: CA360961114

Gene: RAD50

Linked Data

• MyVariant Identifiers: chr5:g.131945085G>C (hg19) ; chr5:g.132609393G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132609393G>C , CM000667.2:g.132609393G>C	GRCh38
NC_000005.9:g.131945085G>C , CM000667.1:g.131945085G>C	GRCh37
NC_000005.8:g.131972984G>C	NCBI36
NG_021151.1:g.57470G>C
NG_021151.2:g.57417G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000378823.8:c.3033G>C MANE Select	ENSP00000368100.4:p.Gln1011His
ENST00000638452.2:c.2736G>C	ENSP00000492349.2:p.Gln912His
ENST00000638504.1:n.2641G>C
ENST00000638568.2:c.2736G>C	ENSP00000491158.2:p.Gln912His
ENST00000639899.1:n.3552G>C
ENST00000640655.2:c.2736G>C	ENSP00000491596.2:p.Gln912His
ENST00000651723.1:c.*3116G>C	ENSP00000498237.1:n.*3116G>C
ENST00000378823.7:c.3033G>C	ENSP00000368100.4:p.Gln1011His
ENST00000533482.5:c.*2659G>C	ENSP00000431225.1:n.*2659G>C
NM_005732.3:c.3033G>C	NP_005723.2:p.Gln1011His
NM_005732.4:c.3033G>C MANE Select	NP_005723.2:p.Gln1011His