Canonical Allele Identifier: CA1583229622

Gene: RAD50

Linked Data

• dbSNP Id: rs1751041232

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132609250_132609251insACC , CM000667.2:g.132609250_132609251insACC	GRCh38
NC_000005.9:g.131944942_131944943insACC , CM000667.1:g.131944942_131944943insACC	GRCh37
NC_000005.8:g.131972841_131972842insACC	NCBI36
NG_021151.1:g.57327_57328insACC
NG_021151.2:g.57274_57275insACC

Transcript Alleles

HGVS	Amino-acid change
ENST00000378823.8:c.2923-33_2923-32insACC MANE Select	ENSP00000368100.4:n.2923-33_2923-32insACC...
ENST00000638452.2:c.2626-33_2626-32insACC	ENSP00000492349.2:n.2626-33_2626-32insACC...
ENST00000638504.1:n.2531-33_2531-32insACC
ENST00000638568.2:c.2626-33_2626-32insACC	ENSP00000491158.2:n.2626-33_2626-32insACC...
ENST00000639899.1:n.3442-33_3442-32insACC
ENST00000640655.2:c.2626-33_2626-32insACC	ENSP00000491596.2:n.2626-33_2626-32insACC...
ENST00000651160.1:c.*1067-33_*1067-32insACC	ENSP00000498829.1:n.*1067-33_*1067-32insA...
ENST00000651723.1:c.*3006-33_*3006-32insACC	ENSP00000498237.1:n.*3006-33_*3006-32insA...
ENST00000378823.7:c.2923-33_2923-32insACC	ENSP00000368100.4:n.2923-33_2923-32insACC...
ENST00000423956.5:c.*1109-33_*1109-32insACC	ENSP00000390971.1:n.*1109-33_*1109-32insA...
ENST00000533482.5:c.*2549-33_*2549-32insACC	ENSP00000431225.1:n.*2549-33_*2549-32insA...
NM_005732.3:c.2923-33_2923-32insACC	NP_005723.2:n.2923-33_2923-32insACC
NM_005732.4:c.2923-33_2923-32insACC MANE Select	NP_005723.2:n.2923-33_2923-32insACC