Canonical Allele Identifier: CA127227674

Gene: RAD50

Linked Data

• dbSNP Id: rs545728592
• gnomAD v3: 5-132565457-G-A
• gnomAD v4: 5-132565457-G-A
• MyVariant Identifiers: chr5:g.131901149G>A (hg19) ; chr5:g.132565457G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132565457G>A , CM000667.2:g.132565457G>A	GRCh38
NC_000005.9:g.131901149G>A , CM000667.1:g.131901149G>A	GRCh37
NC_000005.8:g.131929048G>A	NCBI36
NG_021151.1:g.13534G>A
NG_021151.2:g.13481G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000378823.8:c.213+6090G>A MANE Select	ENSP00000368100.4:n.213+6090G>A
ENST00000638452.2:c.-85+6090G>A	ENSP00000492349.2:n.-85+6090G>A
ENST00000638504.1:n.290+6090G>A
ENST00000638568.2:c.-85+6090G>A	ENSP00000491158.2:n.-85+6090G>A
ENST00000639899.1:n.373+6090G>A
ENST00000640655.2:c.-85+6090G>A	ENSP00000491596.2:n.-85+6090G>A
ENST00000651160.1:c.213+6090G>A	ENSP00000498829.1:n.213+6090G>A
ENST00000651541.1:c.-85+6090G>A	ENSP00000498795.1:n.-85+6090G>A
ENST00000651658.1:n.281+6090G>A
ENST00000651723.1:c.*361+6090G>A	ENSP00000498237.1:n.*361+6090G>A
ENST00000652016.1:c.213+6090G>A	ENSP00000498267.1:n.213+6090G>A
ENST00000652485.1:c.213+6090G>A	ENSP00000498973.1:n.213+6090G>A
ENST00000378823.7:c.213+6090G>A	ENSP00000368100.4:n.213+6090G>A
ENST00000416135.5:c.-85+6090G>A	ENSP00000389515.1:n.-85+6090G>A
ENST00000423956.5:c.213+6090G>A	ENSP00000390971.1:n.213+6090G>A
ENST00000453394.5:c.213+6090G>A	ENSP00000400049.1:n.213+6090G>A
ENST00000533482.5:c.213+6090G>A	ENSP00000431225.1:n.213+6090G>A
NM_005732.3:c.213+6090G>A	NP_005723.2:n.213+6090G>A
NM_005732.4:c.213+6090G>A MANE Select	NP_005723.2:n.213+6090G>A