Canonical Allele Identifier: CA446495333

Gene: RAD50

Linked Data

• MyVariant Identifiers: chr5:g.131945034A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132609342A>G , CM000667.2:g.132609342A>G	GRCh38
NC_000005.9:g.131945034A>G , CM000667.1:g.131945034A>G	GRCh37
NC_000005.8:g.131972933A>G	NCBI36
NG_021151.1:g.57419A>G
NG_021151.2:g.57366A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000378823.8:c.2982A>G MANE Select	ENSP00000368100.4:p.Lys994=
ENST00000638452.2:c.2685A>G	ENSP00000492349.2:p.Lys895=
ENST00000638504.1:n.2590A>G
ENST00000638568.2:c.2685A>G	ENSP00000491158.2:p.Lys895=
ENST00000639899.1:n.3501A>G
ENST00000640655.2:c.2685A>G	ENSP00000491596.2:p.Lys895=
ENST00000651723.1:c.*3065A>G	ENSP00000498237.1:n.*3065A>G
ENST00000378823.7:c.2982A>G	ENSP00000368100.4:p.Lys994=
ENST00000533482.5:c.*2608A>G	ENSP00000431225.1:n.*2608A>G
NM_005732.3:c.2982A>G	NP_005723.2:p.Lys994=
NM_005732.4:c.2982A>G MANE Select	NP_005723.2:p.Lys994=