Canonical Allele Identifier: CA2675215831

Gene: RAD50

Linked Data

• gnomAD v4: 5-132557229-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132557229A>G , CM000667.2:g.132557229A>G	GRCh38
NC_000005.9:g.131892921A>G , CM000667.1:g.131892921A>G	GRCh37
NC_000005.8:g.131920820A>G	NCBI36
NG_021151.1:g.5306A>G
NG_021151.2:g.5253A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000378823.8:c.-96A>G MANE Select	ENSP00000368100.4:n.-96A>G
ENST00000638452.2:c.-168-2055A>G	ENSP00000492349.2:n.-168-2055A>G
ENST00000638504.1:n.207-2055A>G
ENST00000638568.2:c.-169+756A>G	ENSP00000491158.2:n.-169+756A>G
ENST00000639899.1:n.290-2055A>G
ENST00000640655.2:c.-168-2055A>G	ENSP00000491596.2:n.-168-2055A>G
ENST00000651160.1:c.-96A>G	ENSP00000498829.1:n.-96A>G
ENST00000651541.1:c.-169+220A>G	ENSP00000498795.1:n.-169+220A>G
ENST00000651723.1:c.-96A>G	ENSP00000498237.1:n.-96A>G
ENST00000652016.1:c.-96A>G	ENSP00000498267.1:n.-96A>G
ENST00000652485.1:c.-96A>G	ENSP00000498973.1:n.-96A>G
ENST00000378823.7:c.-96A>G	ENSP00000368100.4:n.-96A>G
ENST00000416135.5:c.-169+756A>G	ENSP00000389515.1:n.-169+756A>G
ENST00000533482.5:c.-96A>G	ENSP00000431225.1:n.-96A>G
NM_005732.3:c.-96A>G	NP_005723.2:n.-96A>G
NM_005732.4:c.-96A>G MANE Select	NP_005723.2:n.-96A>G