Canonical Allele Identifier: CA446356675

Gene: RAD50

Linked Data

• ClinVar Variation Id: 2682067
• ClinVar RCV Id: RCV003477359
• MyVariant Identifiers: chr5:g.131915662T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132579970T>C , CM000667.2:g.132579970T>C	GRCh38
NC_000005.9:g.131915662T>C , CM000667.1:g.131915662T>C	GRCh37
NC_000005.8:g.131943561T>C	NCBI36
NG_021151.1:g.28047T>C
NG_021151.2:g.27994T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000378823.8:c.660T>C MANE Select	ENSP00000368100.4:p.Ala220=
ENST00000638452.2:c.363T>C	ENSP00000492349.2:p.Ala121=
ENST00000638504.1:n.442+4042T>C
ENST00000638568.2:c.363T>C	ENSP00000491158.2:p.Ala121=
ENST00000639899.1:n.1179T>C
ENST00000640655.2:c.363T>C	ENSP00000491596.2:p.Ala121=
ENST00000651160.1:c.660T>C	ENSP00000498829.1:p.Ala220=
ENST00000651541.1:c.363T>C	ENSP00000498795.1:p.Ala121=
ENST00000651658.1:n.1087T>C
ENST00000651723.1:c.*743T>C	ENSP00000498237.1:n.*743T>C
ENST00000652016.1:c.660T>C	ENSP00000498267.1:p.Ala220=
ENST00000652485.1:c.660T>C	ENSP00000498973.1:p.Ala220=
ENST00000378823.7:c.660T>C	ENSP00000368100.4:p.Ala220=
ENST00000423956.5:c.660T>C	ENSP00000390971.1:p.Ala220=
ENST00000453394.5:c.660T>C	ENSP00000400049.1:p.Ala220=
ENST00000487596.1:n.226T>C
ENST00000533482.5:c.*286T>C	ENSP00000431225.1:n.*286T>C
NM_005732.3:c.660T>C	NP_005723.2:p.Ala220=
NM_005732.4:c.660T>C MANE Select	NP_005723.2:p.Ala220=