Canonical Allele Identifier: CA360946505

Gene: RAD50

Linked Data

• MyVariant Identifiers: chr5:g.131927654A>C (hg19) ; chr5:g.132591962A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132591962A>C , CM000667.2:g.132591962A>C	GRCh38
NC_000005.9:g.131927654A>C , CM000667.1:g.131927654A>C	GRCh37
NC_000005.8:g.131955553A>C	NCBI36
NG_021151.1:g.40039A>C
NG_021151.2:g.39986A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.1721A>C MANE Select	ENSP00000368100.4:p.Lys574Thr
ENST00000638452.2:c.1424A>C	ENSP00000492349.2:p.Lys475Thr
ENST00000638504.1:n.1407A>C
ENST00000638568.2:c.1424A>C	ENSP00000491158.2:p.Lys475Thr
ENST00000639899.1:n.2240A>C
ENST00000640655.2:c.1424A>C	ENSP00000491596.2:p.Lys475Thr
ENST00000651160.1:c.1721A>C	ENSP00000498829.1:p.Lys574Thr
ENST00000651541.1:c.1424A>C	ENSP00000498795.1:p.Lys475Thr
ENST00000651658.1:n.2148A>C
ENST00000651723.1:c.*1804A>C	ENSP00000498237.1:n.*1804A>C
ENST00000652016.1:c.1721A>C	ENSP00000498267.1:p.Lys574Thr
ENST00000652485.1:c.1754A>C	ENSP00000498973.1:p.Lys585Thr
ENST00000378823.7:c.1721A>C	ENSP00000368100.4:p.Lys574Thr
ENST00000423956.5:c.1635+556A>C	ENSP00000390971.1:n.1635+556A>C
ENST00000434288.1:c.216A>C
ENST00000453394.5:c.1538A>C	ENSP00000400049.1:p.Lys513Thr
ENST00000533482.5:c.*1347A>C	ENSP00000431225.1:n.*1347A>C
NM_005732.3:c.1721A>C	NP_005723.2:p.Lys574Thr
NM_005732.4:c.1721A>C MANE Select	NP_005723.2:p.Lys574Thr