Canonical Allele Identifier: CA360934632

Gene: RAD50

Linked Data

• MyVariant Identifiers: chr5:g.131915139T>A (hg19) ; chr5:g.132579447T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132579447T>A , CM000667.2:g.132579447T>A	GRCh38
NC_000005.9:g.131915139T>A , CM000667.1:g.131915139T>A	GRCh37
NC_000005.8:g.131943038T>A	NCBI36
NG_021151.1:g.27524T>A
NG_021151.2:g.27471T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.496T>A MANE Select	ENSP00000368100.4:p.Leu166Ile
ENST00000638452.2:c.199T>A	ENSP00000492349.2:p.Leu67Ile
ENST00000638504.1:n.442+3519T>A
ENST00000638568.2:c.199T>A	ENSP00000491158.2:p.Leu67Ile
ENST00000639899.1:n.656T>A
ENST00000640655.2:c.199T>A	ENSP00000491596.2:p.Leu67Ile
ENST00000651160.1:c.496T>A	ENSP00000498829.1:p.Leu166Ile
ENST00000651541.1:c.199T>A	ENSP00000498795.1:p.Leu67Ile
ENST00000651658.1:n.564T>A
ENST00000651723.1:c.*579T>A	ENSP00000498237.1:n.*579T>A
ENST00000652016.1:c.496T>A	ENSP00000498267.1:p.Leu166Ile
ENST00000652485.1:c.496T>A	ENSP00000498973.1:p.Leu166Ile
ENST00000378823.7:c.496T>A	ENSP00000368100.4:p.Leu166Ile
ENST00000416135.5:c.199T>A	ENSP00000389515.1:p.Leu67Ile
ENST00000423956.5:c.496T>A	ENSP00000390971.1:p.Leu166Ile
ENST00000453394.5:c.496T>A	ENSP00000400049.1:p.Leu166Ile
ENST00000533482.5:c.*122T>A	ENSP00000431225.1:n.*122T>A
NM_005732.3:c.496T>A	NP_005723.2:p.Leu166Ile
NM_005732.4:c.496T>A MANE Select	NP_005723.2:p.Leu166Ile