Canonical Allele Identifier: CA2710356523
Gene: RAD50 HGNC NCBI

Linked Data

dbSNP Id: rs2149836490

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132575934T>A , CM000667.2:g.132575934T>A GRCh38
NC_000005.9:g.131911626T>A , CM000667.1:g.131911626T>A GRCh37
NC_000005.8:g.131939525T>A NCBI36
NG_021151.1:g.24011T>A
NG_021151.2:g.23958T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378823.8:c.365+6T>A MANE Select ENSP00000368100.4:n.365+6T>A
ENST00000638452.2:c.68+6T>A ENSP00000492349.2:n.68+6T>A
ENST00000638504.1:n.442+6T>A
ENST00000638568.2:c.68+6T>A ENSP00000491158.2:n.68+6T>A
ENST00000639899.1:n.525+6T>A
ENST00000640655.2:c.68+6T>A ENSP00000491596.2:n.68+6T>A
ENST00000651160.1:c.365+6T>A ENSP00000498829.1:n.365+6T>A
ENST00000651541.1:c.68+6T>A ENSP00000498795.1:n.68+6T>A
ENST00000651658.1:n.433+6T>A
ENST00000651723.1:c.*448+71T>A ENSP00000498237.1:n.*448+71T>A
ENST00000652016.1:c.365+6T>A ENSP00000498267.1:n.365+6T>A
ENST00000652485.1:c.365+6T>A ENSP00000498973.1:n.365+6T>A
ENST00000378823.7:c.365+6T>A ENSP00000368100.4:n.365+6T>A
ENST00000416135.5:c.68+6T>A ENSP00000389515.1:n.68+6T>A
ENST00000423956.5:c.365+6T>A ENSP00000390971.1:n.365+6T>A
ENST00000453394.5:c.365+6T>A ENSP00000400049.1:n.365+6T>A
ENST00000533482.5:c.300+71T>A ENSP00000431225.1:n.300+71T>A
NM_005732.3:c.365+6T>A NP_005723.2:n.365+6T>A
NM_005732.4:c.365+6T>A MANE Select NP_005723.2:n.365+6T>A