Canonical Allele Identifier: CA360961132

Gene: RAD50

Linked Data

• MyVariant Identifiers: chr5:g.131945088G>T (hg19) ; chr5:g.132609396G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132609396G>T , CM000667.2:g.132609396G>T	GRCh38
NC_000005.9:g.131945088G>T , CM000667.1:g.131945088G>T	GRCh37
NC_000005.8:g.131972987G>T	NCBI36
NG_021151.1:g.57473G>T
NG_021151.2:g.57420G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000378823.8:c.3036G>T MANE Select	ENSP00000368100.4:p.Lys1012Asn
ENST00000638452.2:c.2739G>T	ENSP00000492349.2:p.Lys913Asn
ENST00000638504.1:n.2644G>T
ENST00000638568.2:c.2739G>T	ENSP00000491158.2:p.Lys913Asn
ENST00000639899.1:n.3555G>T
ENST00000640655.2:c.2739G>T	ENSP00000491596.2:p.Lys913Asn
ENST00000651723.1:c.*3119G>T	ENSP00000498237.1:n.*3119G>T
ENST00000378823.7:c.3036G>T	ENSP00000368100.4:p.Lys1012Asn
ENST00000533482.5:c.*2662G>T	ENSP00000431225.1:n.*2662G>T
NM_005732.3:c.3036G>T	NP_005723.2:p.Lys1012Asn
NM_005732.4:c.3036G>T MANE Select	NP_005723.2:p.Lys1012Asn