Canonical Allele Identifier: CA446361256

Gene: RAD50

Linked Data

• MyVariant Identifiers: chr5:g.131925499T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132589807T>A , CM000667.2:g.132589807T>A	GRCh38
NC_000005.9:g.131925499T>A , CM000667.1:g.131925499T>A	GRCh37
NC_000005.8:g.131953398T>A	NCBI36
NG_021151.1:g.37884T>A
NG_021151.2:g.37831T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.1422T>A MANE Select	ENSP00000368100.4:p.Ile474=
ENST00000638452.2:c.1125T>A	ENSP00000492349.2:p.Ile375=
ENST00000638504.1:n.1108T>A
ENST00000638568.2:c.1125T>A	ENSP00000491158.2:p.Ile375=
ENST00000639899.1:n.1941T>A
ENST00000640655.2:c.1125T>A	ENSP00000491596.2:p.Ile375=
ENST00000651160.1:c.1422T>A	ENSP00000498829.1:p.Ile474=
ENST00000651541.1:c.1125T>A	ENSP00000498795.1:p.Ile375=
ENST00000651658.1:n.1849T>A
ENST00000651723.1:c.*1505T>A	ENSP00000498237.1:n.*1505T>A
ENST00000652016.1:c.1422T>A	ENSP00000498267.1:p.Ile474=
ENST00000652485.1:c.1422T>A	ENSP00000498973.1:p.Ile474=
ENST00000378823.7:c.1422T>A	ENSP00000368100.4:p.Ile474=
ENST00000423956.5:c.1422T>A	ENSP00000390971.1:p.Ile474=
ENST00000453394.5:c.1422T>A	ENSP00000400049.1:p.Ile474=
ENST00000533482.5:c.*1048T>A	ENSP00000431225.1:n.*1048T>A
NM_005732.3:c.1422T>A	NP_005723.2:p.Ile474=
NM_005732.4:c.1422T>A MANE Select	NP_005723.2:p.Ile474=