Canonical Allele Identifier: CA360933211

Gene: RAD50

Linked Data

• gnomAD v4: 5-132579318-C-G
• MyVariant Identifiers: chr5:g.131915010C>G (hg19) ; chr5:g.132579318C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132579318C>G , CM000667.2:g.132579318C>G	GRCh38
NC_000005.9:g.131915010C>G , CM000667.1:g.131915010C>G	GRCh37
NC_000005.8:g.131942909C>G	NCBI36
NG_021151.1:g.27395C>G
NG_021151.2:g.27342C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.367C>G MANE Select	ENSP00000368100.4:p.His123Asp
ENST00000638452.2:c.70C>G	ENSP00000492349.2:p.His24Asp
ENST00000638504.1:n.442+3390C>G
ENST00000638568.2:c.70C>G	ENSP00000491158.2:p.His24Asp
ENST00000639899.1:n.527C>G
ENST00000640655.2:c.70C>G	ENSP00000491596.2:p.His24Asp
ENST00000651160.1:c.367C>G	ENSP00000498829.1:p.His123Asp
ENST00000651541.1:c.70C>G	ENSP00000498795.1:p.His24Asp
ENST00000651658.1:n.435C>G
ENST00000651723.1:c.*450C>G	ENSP00000498237.1:n.*450C>G
ENST00000652016.1:c.367C>G	ENSP00000498267.1:p.His123Asp
ENST00000652485.1:c.367C>G	ENSP00000498973.1:p.His123Asp
ENST00000378823.7:c.367C>G	ENSP00000368100.4:p.His123Asp
ENST00000416135.5:c.70C>G	ENSP00000389515.1:p.His24Asp
ENST00000423956.5:c.367C>G	ENSP00000390971.1:p.His123Asp
ENST00000453394.5:c.367C>G	ENSP00000400049.1:p.His123Asp
ENST00000533482.5:c.302C>G	ENSP00000431225.1:p.Ala101Gly
NM_005732.3:c.367C>G	NP_005723.2:p.His123Asp
NM_005732.4:c.367C>G MANE Select	NP_005723.2:p.His123Asp