Canonical Allele Identifier: CA446361160

Gene: RAD50

Linked Data

• gnomAD v4: 5-132589642-A-C
• MyVariant Identifiers: chr5:g.131925334A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132589642A>C , CM000667.2:g.132589642A>C	GRCh38
NC_000005.9:g.131925334A>C , CM000667.1:g.131925334A>C	GRCh37
NC_000005.8:g.131953233A>C	NCBI36
NG_021151.1:g.37719A>C
NG_021151.2:g.37666A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000378823.8:c.1257A>C MANE Select	ENSP00000368100.4:p.Ala419=
ENST00000638452.2:c.960A>C	ENSP00000492349.2:p.Ala320=
ENST00000638504.1:n.943A>C
ENST00000638568.2:c.960A>C	ENSP00000491158.2:p.Ala320=
ENST00000639899.1:n.1776A>C
ENST00000640655.2:c.960A>C	ENSP00000491596.2:p.Ala320=
ENST00000651160.1:c.1257A>C	ENSP00000498829.1:p.Ala419=
ENST00000651541.1:c.960A>C	ENSP00000498795.1:p.Ala320=
ENST00000651658.1:n.1684A>C
ENST00000651723.1:c.*1340A>C	ENSP00000498237.1:n.*1340A>C
ENST00000652016.1:c.1257A>C	ENSP00000498267.1:p.Ala419=
ENST00000652485.1:c.1257A>C	ENSP00000498973.1:p.Ala419=
ENST00000378823.7:c.1257A>C	ENSP00000368100.4:p.Ala419=
ENST00000423956.5:c.1257A>C	ENSP00000390971.1:p.Ala419=
ENST00000453394.5:c.1257A>C	ENSP00000400049.1:p.Ala419=
ENST00000533482.5:c.*883A>C	ENSP00000431225.1:n.*883A>C
NM_005732.3:c.1257A>C	NP_005723.2:p.Ala419=
NM_005732.4:c.1257A>C MANE Select	NP_005723.2:p.Ala419=