Canonical Allele Identifier: CA2615861761
Gene: ATM HGNC NCBI
C11orf65 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108310129_108310131del , CM000673.2:g.108310129_108310131del GRCh38
NC_000011.9:g.108180856_108180858del , CM000673.1:g.108180856_108180858del GRCh37
NC_000011.8:g.107686066_107686068del NCBI36
NG_009830.1:g.92298_92300del , LRG_135:g.92298_92300del
NG_054724.1:g.164702_164704del

Transcript Alleles

HGVS Amino-acid Change
ENST00000452508.7:c.5763-31_5763-29del (ATM) ENSP00000388058.2:n.5763-31_5763-29del
ENST00000713593.1:c.*5234-31_*5234-29del (ATM) ENSP00000518889.1:n.*5234-31_*5234-29del
ENST00000278616.9:c.5763-31_5763-29del (ATM) ENSP00000278616.4:n.5763-31_5763-29del
ENST00000525056.2:n.182-31_182-29del (ATM)
ENST00000682286.1:n.520-31_520-29del (ATM)
ENST00000682302.1:n.181-31_181-29del (ATM)
ENST00000683174.1:n.7247-31_7247-29del (ATM)
ENST00000683524.1:n.987-31_987-29del (ATM)
ENST00000684152.1:n.1477-31_1477-29del (ATM)
ENST00000527805.6:c.*827-31_*827-29del (ATM) ENSP00000435747.2:n.*827-31_*827-29del
ENST00000675595.1:c.*827-31_*827-29del (ATM) ENSP00000502563.1:n.*827-31_*827-29del
ENST00000675843.1:c.5763-31_5763-29del (ATM) MANE Select ENSP00000501606.1:n.5763-31_5763-29del
ENST00000278616.8:c.5763-31_5763-29del (ATM) ENSP00000278616.4:n.5763-31_5763-29del
ENST00000452508.6:c.5763-31_5763-29del (ATM) ENSP00000388058.2:n.5763-31_5763-29del
ENST00000524792.5:n.1978-31_1978-29del (ATM)
ENST00000525729.5:c.641-1060_641-1058del (C11orf65) ENSP00000433395.1:n.641-1060_641-1058del
ENST00000529588.5:c.187-31_187-29del (ATM)
ENST00000532765.1:n.80-31_80-29del (ATM)
ENST00000533690.5:n.1167-31_1167-29del (ATM)
NM_000051.3:c.5763-31_5763-29del , LRG_135t1:c.5763-31_5763-29del (ATM) NP_000042.3:n.5763-31_5763-29del
XM_005271561.3:c.5763-31_5763-29del (ATM) XP_005271618.2:n.5763-31_5763-29del
XM_005271562.3:c.5763-31_5763-29del (ATM) XP_005271619.2:n.5763-31_5763-29del
XM_006718843.2:c.5763-31_5763-29del (ATM) XP_006718906.1:n.5763-31_5763-29del
XM_006718845.1:c.1719-31_1719-29del (ATM) XP_006718908.1:n.1719-31_1719-29del
XM_011542840.1:c.5763-31_5763-29del (ATM) XP_011541142.1:n.5763-31_5763-29del
XM_011542841.1:c.5763-31_5763-29del (ATM) XP_011541143.1:n.5763-31_5763-29del
XM_011542842.1:c.5598-31_5598-29del (ATM) XP_011541144.1:n.5598-31_5598-29del
XM_011542843.1:c.5763-31_5763-29del (ATM) XP_011541145.1:n.5763-31_5763-29del
XM_011542844.1:c.4719-31_4719-29del (ATM) XP_011541146.1:n.4719-31_4719-29del
XM_011542845.1:c.4455-31_4455-29del (ATM) XP_011541147.1:n.4455-31_4455-29del
XM_011542847.1:c.834-31_834-29del (ATM) XP_011541149.1:n.834-31_834-29del
NM_001330368.1:c.641-1060_641-1058del (C11orf65) NP_001317297.1:n.641-1060_641-1058del
NM_001351110.1:c.*39-1060_*39-1058del (C11orf65) NP_001338039.1:n.*39-1060_*39-1058del
NM_001351834.1:c.5763-31_5763-29del (ATM) NP_001338763.1:n.5763-31_5763-29del
XM_005271562.5:c.5763-31_5763-29del (ATM) XP_005271619.2:n.5763-31_5763-29del
XM_006718843.4:c.5763-31_5763-29del (ATM) XP_006718906.1:n.5763-31_5763-29del
XM_006718845.2:c.1719-31_1719-29del (ATM) XP_006718908.1:n.1719-31_1719-29del
XM_011542840.3:c.5763-31_5763-29del (ATM) XP_011541142.1:n.5763-31_5763-29del
XM_011542842.3:c.5598-31_5598-29del (ATM) XP_011541144.1:n.5598-31_5598-29del
XM_011542843.2:c.5763-31_5763-29del (ATM) XP_011541145.1:n.5763-31_5763-29del
XM_011542844.3:c.4719-31_4719-29del (ATM) XP_011541146.1:n.4719-31_4719-29del
XM_011542845.2:c.4455-31_4455-29del (ATM) XP_011541147.1:n.4455-31_4455-29del
XM_017017789.2:c.5763-31_5763-29del (ATM) XP_016873278.1:n.5763-31_5763-29del
XM_017017790.2:c.5763-31_5763-29del (ATM) XP_016873279.1:n.5763-31_5763-29del
XM_017017791.1:c.5763-31_5763-29del (ATM) XP_016873280.1:n.5763-31_5763-29del
XR_002957150.1:n.6363-31_6363-29del (ATM)
NM_001330368.2:c.641-1060_641-1058del (C11orf65) NP_001317297.1:n.641-1060_641-1058del
NM_001351110.2:c.*39-1060_*39-1058del (C11orf65) NP_001338039.1:n.*39-1060_*39-1058del
NM_001351834.2:c.5763-31_5763-29del (ATM) NP_001338763.1:n.5763-31_5763-29del
NM_000051.4:c.5763-31_5763-29del (ATM) MANE Select NP_000042.3:n.5763-31_5763-29del