Canonical Allele Identifier: CA446363942

Gene: RAD50

Linked Data

• MyVariant Identifiers: chr5:g.131940499T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132604807T>A , CM000667.2:g.132604807T>A	GRCh38
NC_000005.9:g.131940499T>A , CM000667.1:g.131940499T>A	GRCh37
NC_000005.8:g.131968398T>A	NCBI36
NG_021151.1:g.52884T>A
NG_021151.2:g.52831T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000378823.8:c.2526T>A MANE Select	ENSP00000368100.4:p.Val842=
ENST00000638452.2:c.2229T>A	ENSP00000492349.2:p.Val743=
ENST00000638504.1:n.2134T>A
ENST00000638568.2:c.2229T>A	ENSP00000491158.2:p.Val743=
ENST00000639899.1:n.3045T>A
ENST00000640655.2:c.2229T>A	ENSP00000491596.2:p.Val743=
ENST00000651160.1:c.*670T>A	ENSP00000498829.1:n.*670T>A
ENST00000651723.1:c.*2609T>A	ENSP00000498237.1:n.*2609T>A
ENST00000652016.1:c.*743T>A	ENSP00000498267.1:n.*743T>A
ENST00000652485.1:c.2559T>A	ENSP00000498973.1:p.Val853=
ENST00000378823.7:c.2526T>A	ENSP00000368100.4:p.Val842=
ENST00000423956.5:c.*712T>A	ENSP00000390971.1:n.*712T>A
ENST00000533482.5:c.*2152T>A	ENSP00000431225.1:n.*2152T>A
NM_005732.3:c.2526T>A	NP_005723.2:p.Val842=
NM_005732.4:c.2526T>A MANE Select	NP_005723.2:p.Val842=