Canonical Allele Identifier: CA360951013
Gene: RAD50 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132557369T>A , CM000667.2:g.132557369T>A GRCh38
NC_000005.9:g.131893061T>A , CM000667.1:g.131893061T>A GRCh37
NC_000005.8:g.131920960T>A NCBI36
NG_021151.1:g.5446T>A
NG_021151.2:g.5393T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000378823.8:c.45T>A MANE Select ENSP00000368100.4:p.Phe15Leu
ENST00000638452.2:c.-168-1915T>A ENSP00000492349.2:n.-168-1915T>A
ENST00000638504.1:n.207-1915T>A
ENST00000638568.2:c.-169+896T>A ENSP00000491158.2:n.-169+896T>A
ENST00000639899.1:n.290-1915T>A
ENST00000640655.2:c.-168-1915T>A ENSP00000491596.2:n.-168-1915T>A
ENST00000651160.1:c.45T>A ENSP00000498829.1:p.Phe15Leu
ENST00000651541.1:c.-169+360T>A ENSP00000498795.1:n.-169+360T>A
ENST00000651658.1:n.113T>A
ENST00000651723.1:c.45T>A ENSP00000498237.1:p.Phe15Leu
ENST00000652016.1:c.45T>A ENSP00000498267.1:p.Phe15Leu
ENST00000652485.1:c.45T>A ENSP00000498973.1:p.Phe15Leu
ENST00000378823.7:c.45T>A ENSP00000368100.4:p.Phe15Leu
ENST00000416135.5:c.-169+896T>A ENSP00000389515.1:n.-169+896T>A
ENST00000423956.5:c.45T>A ENSP00000390971.1:p.Phe15Leu
ENST00000453394.5:c.45T>A ENSP00000400049.1:p.Phe15Leu
ENST00000533482.5:c.45T>A ENSP00000431225.1:p.Phe15Leu
NM_005732.3:c.45T>A NP_005723.2:p.Phe15Leu
NM_005732.4:c.45T>A MANE Select NP_005723.2:p.Phe15Leu