Canonical Allele Identifier: CA360956720

Gene: RAD50

Linked Data

• MyVariant Identifiers: chr5:g.131940620C>G (hg19) ; chr5:g.132604928C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132604928C>G , CM000667.2:g.132604928C>G	GRCh38
NC_000005.9:g.131940620C>G , CM000667.1:g.131940620C>G	GRCh37
NC_000005.8:g.131968519C>G	NCBI36
NG_021151.1:g.53005C>G
NG_021151.2:g.52952C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.2647C>G MANE Select	ENSP00000368100.4:p.Arg883Gly
ENST00000638452.2:c.2350C>G	ENSP00000492349.2:p.Arg784Gly
ENST00000638504.1:n.2255C>G
ENST00000638568.2:c.2350C>G	ENSP00000491158.2:p.Arg784Gly
ENST00000639899.1:n.3166C>G
ENST00000640655.2:c.2350C>G	ENSP00000491596.2:p.Arg784Gly
ENST00000651160.1:c.*791C>G	ENSP00000498829.1:n.*791C>G
ENST00000651723.1:c.*2730C>G	ENSP00000498237.1:n.*2730C>G
ENST00000652016.1:c.*864C>G	ENSP00000498267.1:n.*864C>G
ENST00000652485.1:c.2680C>G	ENSP00000498973.1:p.Arg894Gly
ENST00000378823.7:c.2647C>G	ENSP00000368100.4:p.Arg883Gly
ENST00000423956.5:c.*833C>G	ENSP00000390971.1:n.*833C>G
ENST00000533482.5:c.*2273C>G	ENSP00000431225.1:n.*2273C>G
NM_005732.3:c.2647C>G	NP_005723.2:p.Arg883Gly
NM_005732.4:c.2647C>G MANE Select	NP_005723.2:p.Arg883Gly