Canonical Allele Identifier: CA1583229712
Gene: RAD50 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132609404_132609405delinsTG , CM000667.2:g.132609404_132609405delinsTG GRCh38
NC_000005.9:g.131945096_131945097delinsTG , CM000667.1:g.131945096_131945097delinsTG GRCh37
NC_000005.8:g.131972995_131972996delinsTG NCBI36
NG_021151.1:g.57481_57482delinsTG
NG_021151.2:g.57428_57429delinsTG

Transcript Alleles

HGVS Amino-acid change
ENST00000378823.8:c.3036+8_3036+9delinsTG MANE Select ENSP00000368100.4:n.3036+8_3036+9delinsTG...
ENST00000638452.2:c.2739+8_2739+9delinsTG ENSP00000492349.2:n.2739+8_2739+9delinsTG...
ENST00000638504.1:n.2644+8_2644+9delinsTG
ENST00000638568.2:c.2739+8_2739+9delinsTG ENSP00000491158.2:n.2739+8_2739+9delinsTG...
ENST00000639899.1:n.3555+8_3555+9delinsTG
ENST00000640655.2:c.2739+8_2739+9delinsTG ENSP00000491596.2:n.2739+8_2739+9delinsTG...
ENST00000651723.1:c.*3119+8_*3119+9delinsTG ENSP00000498237.1:n.*3119+8_*3119+9delins...
ENST00000378823.7:c.3036+8_3036+9delinsTG ENSP00000368100.4:n.3036+8_3036+9delinsTG...
ENST00000533482.5:c.*2662+8_*2662+9delinsTG ENSP00000431225.1:n.*2662+8_*2662+9delins...
NM_005732.3:c.3036+8_3036+9delinsTG NP_005723.2:n.3036+8_3036+9delinsTG
NM_005732.4:c.3036+8_3036+9delinsTG MANE Select NP_005723.2:n.3036+8_3036+9delinsTG