Canonical Allele Identifier: CA360956707

Gene: RAD50

Linked Data

• dbSNP Id: rs2149847808
• MyVariant Identifiers: chr5:g.131940617C>T (hg19) ; chr5:g.132604925C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132604925C>T , CM000667.2:g.132604925C>T	GRCh38
NC_000005.9:g.131940617C>T , CM000667.1:g.131940617C>T	GRCh37
NC_000005.8:g.131968516C>T	NCBI36
NG_021151.1:g.53002C>T
NG_021151.2:g.52949C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.2644C>T MANE Select	ENSP00000368100.4:p.Gln882Ter
ENST00000638452.2:c.2347C>T	ENSP00000492349.2:p.Gln783Ter
ENST00000638504.1:n.2252C>T
ENST00000638568.2:c.2347C>T	ENSP00000491158.2:p.Gln783Ter
ENST00000639899.1:n.3163C>T
ENST00000640655.2:c.2347C>T	ENSP00000491596.2:p.Gln783Ter
ENST00000651160.1:c.*788C>T	ENSP00000498829.1:n.*788C>T
ENST00000651723.1:c.*2727C>T	ENSP00000498237.1:n.*2727C>T
ENST00000652016.1:c.*861C>T	ENSP00000498267.1:n.*861C>T
ENST00000652485.1:c.2677C>T	ENSP00000498973.1:p.Gln893Ter
ENST00000378823.7:c.2644C>T	ENSP00000368100.4:p.Gln882Ter
ENST00000423956.5:c.*830C>T	ENSP00000390971.1:n.*830C>T
ENST00000533482.5:c.*2270C>T	ENSP00000431225.1:n.*2270C>T
NM_005732.3:c.2644C>T	NP_005723.2:p.Gln882Ter
NM_005732.4:c.2644C>T MANE Select	NP_005723.2:p.Gln882Ter