Canonical Allele Identifier: CA1583227059
Gene: RAD50 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132579800G= , CM000667.2:g.132579800G= GRCh38
NC_000005.9:g.131915492G= , CM000667.1:g.131915492G= GRCh37
NC_000005.8:g.131943391G= NCBI36
NG_021151.1:g.27877G=
NG_021151.2:g.27824G=

Transcript Alleles

HGVS Amino-acid change
ENST00000378823.8:c.552-62G= MANE Select ENSP00000368100.4:n.552-62G=
ENST00000638452.2:c.255-62G= ENSP00000492349.2:n.255-62G=
ENST00000638504.1:n.442+3872G=
ENST00000638568.2:c.255-62G= ENSP00000491158.2:n.255-62G=
ENST00000639899.1:n.1009G=
ENST00000640655.2:c.255-62G= ENSP00000491596.2:n.255-62G=
ENST00000651160.1:c.552-62G= ENSP00000498829.1:n.552-62G=
ENST00000651541.1:c.255-62G= ENSP00000498795.1:n.255-62G=
ENST00000651658.1:n.917G=
ENST00000651723.1:c.*635-62G= ENSP00000498237.1:n.*635-62G=
ENST00000652016.1:c.552-62G= ENSP00000498267.1:n.552-62G=
ENST00000652485.1:c.552-62G= ENSP00000498973.1:n.552-62G=
ENST00000378823.7:c.552-62G= ENSP00000368100.4:n.552-62G=
ENST00000416135.5:c.255-62G= ENSP00000389515.1:n.255-62G=
ENST00000423956.5:c.552-62G= ENSP00000390971.1:n.552-62G=
ENST00000453394.5:c.552-62G= ENSP00000400049.1:n.552-62G=
ENST00000487596.1:n.56G=
ENST00000533482.5:c.*178-62G= ENSP00000431225.1:n.*178-62G=
NM_005732.3:c.552-62G= NP_005723.2:n.552-62G=
NM_005732.4:c.552-62G= MANE Select NP_005723.2:n.552-62G=