Canonical Allele Identifier: CA2675215836

Gene: RAD50

Linked Data

• gnomAD v4: 5-132557237-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132557237G>T , CM000667.2:g.132557237G>T	GRCh38
NC_000005.9:g.131892929G>T , CM000667.1:g.131892929G>T	GRCh37
NC_000005.8:g.131920828G>T	NCBI36
NG_021151.1:g.5314G>T
NG_021151.2:g.5261G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000378823.8:c.-88G>T MANE Select	ENSP00000368100.4:n.-88G>T
ENST00000638452.2:c.-168-2047G>T	ENSP00000492349.2:n.-168-2047G>T
ENST00000638504.1:n.207-2047G>T
ENST00000638568.2:c.-169+764G>T	ENSP00000491158.2:n.-169+764G>T
ENST00000639899.1:n.290-2047G>T
ENST00000640655.2:c.-168-2047G>T	ENSP00000491596.2:n.-168-2047G>T
ENST00000651160.1:c.-88G>T	ENSP00000498829.1:n.-88G>T
ENST00000651541.1:c.-169+228G>T	ENSP00000498795.1:n.-169+228G>T
ENST00000651723.1:c.-88G>T	ENSP00000498237.1:n.-88G>T
ENST00000652016.1:c.-88G>T	ENSP00000498267.1:n.-88G>T
ENST00000652485.1:c.-88G>T	ENSP00000498973.1:n.-88G>T
ENST00000378823.7:c.-88G>T	ENSP00000368100.4:n.-88G>T
ENST00000416135.5:c.-169+764G>T	ENSP00000389515.1:n.-169+764G>T
ENST00000423956.5:c.-88G>T	ENSP00000390971.1:n.-88G>T
ENST00000453394.5:c.-88G>T	ENSP00000400049.1:n.-88G>T
ENST00000533482.5:c.-88G>T	ENSP00000431225.1:n.-88G>T
NM_005732.3:c.-88G>T	NP_005723.2:n.-88G>T
NM_005732.4:c.-88G>T MANE Select	NP_005723.2:n.-88G>T