Canonical Allele Identifier: CA1583233438

Gene: RAD50

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132618031_132618032delinsTA , CM000667.2:g.132618031_132618032delinsTA	GRCh38
NC_000005.9:g.131953723_131953724delinsTA , CM000667.1:g.131953723_131953724delinsTA	GRCh37
NC_000005.8:g.131981622_131981623delinsTA	NCBI36
NG_021151.1:g.66108_66109delinsTA
NG_021151.2:g.66055_66056delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.3165-39_3165-38delinsTA MANE Select	ENSP00000368100.4:n.3165-39_3165-38delinsTA
ENST00000638452.2:c.2868-39_2868-38delinsTA	ENSP00000492349.2:n.2868-39_2868-38delinsTA
ENST00000638504.1:n.2773-39_2773-38delinsTA
ENST00000638568.2:c.2868-39_2868-38delinsTA	ENSP00000491158.2:n.2868-39_2868-38delinsTA
ENST00000639899.1:n.3684-39_3684-38delinsTA
ENST00000640655.2:c.2868-39_2868-38delinsTA	ENSP00000491596.2:n.2868-39_2868-38delinsTA
ENST00000378823.7:c.3165-39_3165-38delinsTA	ENSP00000368100.4:n.3165-39_3165-38delinsTA
ENST00000533482.5:c.*2791-39_*2791-38delinsTA	ENSP00000431225.1:n.*2791-39_*2791-38delinsTA
NM_005732.3:c.3165-39_3165-38delinsTA	NP_005723.2:n.3165-39_3165-38delinsTA
NM_005732.4:c.3165-39_3165-38delinsTA MANE Select	NP_005723.2:n.3165-39_3165-38delinsTA