Canonical Allele Identifier: CA127237685

Gene: RAD50

Linked Data

• dbSNP Id: rs569508766
• gnomAD v3: 5-132579793-T-G
• gnomAD v4: 5-132579793-T-G
• MyVariant Identifiers: chr5:g.131915485T>G (hg19) ; chr5:g.132579793T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132579793T>G , CM000667.2:g.132579793T>G	GRCh38
NC_000005.9:g.131915485T>G , CM000667.1:g.131915485T>G	GRCh37
NC_000005.8:g.131943384T>G	NCBI36
NG_021151.1:g.27870T>G
NG_021151.2:g.27817T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000378823.8:c.552-69T>G MANE Select	ENSP00000368100.4:n.552-69T>G
ENST00000638452.2:c.255-69T>G	ENSP00000492349.2:n.255-69T>G
ENST00000638504.1:n.442+3865T>G
ENST00000638568.2:c.255-69T>G	ENSP00000491158.2:n.255-69T>G
ENST00000639899.1:n.1002T>G
ENST00000640655.2:c.255-69T>G	ENSP00000491596.2:n.255-69T>G
ENST00000651160.1:c.552-69T>G	ENSP00000498829.1:n.552-69T>G
ENST00000651541.1:c.255-69T>G	ENSP00000498795.1:n.255-69T>G
ENST00000651658.1:n.910T>G
ENST00000651723.1:c.*635-69T>G	ENSP00000498237.1:n.*635-69T>G
ENST00000652016.1:c.552-69T>G	ENSP00000498267.1:n.552-69T>G
ENST00000652485.1:c.552-69T>G	ENSP00000498973.1:n.552-69T>G
ENST00000378823.7:c.552-69T>G	ENSP00000368100.4:n.552-69T>G
ENST00000416135.5:c.255-69T>G	ENSP00000389515.1:n.255-69T>G
ENST00000423956.5:c.552-69T>G	ENSP00000390971.1:n.552-69T>G
ENST00000453394.5:c.552-69T>G	ENSP00000400049.1:n.552-69T>G
ENST00000487596.1:n.49T>G
ENST00000533482.5:c.*178-69T>G	ENSP00000431225.1:n.*178-69T>G
NM_005732.3:c.552-69T>G	NP_005723.2:n.552-69T>G
NM_005732.4:c.552-69T>G MANE Select	NP_005723.2:n.552-69T>G