Canonical Allele Identifier: CA10579278
Gene: ATM HGNC NCBI
C11orf65 HGNC NCBI

Linked Data

ClinVar Variation Id: 233938
dbSNP Id: rs876660743

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108333947_108333949del , CM000673.2:g.108333947_108333949del GRCh38
NC_000011.9:g.108204674_108204676del , CM000673.1:g.108204674_108204676del GRCh37
NC_000011.8:g.107709884_107709886del NCBI36
NG_009830.1:g.116116_116118del , LRG_135:g.116116_116118del
NG_054724.1:g.140890_140892del

Transcript Alleles

HGVS Amino-acid change
ENST00000452508.7:c.7989_7991del (ATM) ENSP00000388058.2:p.Val2664del
ENST00000713593.1:c.*7460_*7462del (ATM) ENSP00000518889.1:n.*7460_*7462del
ENST00000278616.9:c.7989_7991del (ATM) ENSP00000278616.4:p.Val2664del
ENST00000525056.2:n.2408_2410del (ATM)
ENST00000638786.2:n.687_689del (ATM)
ENST00000682286.1:n.2746_2748del (ATM)
ENST00000682302.1:n.2407_2409del (ATM)
ENST00000683174.1:n.9473_9475del (ATM)
ENST00000683524.1:n.3213_3215del (ATM)
ENST00000684152.1:n.3405_3407del (ATM)
ENST00000684180.1:n.463_465del (ATM)
ENST00000684447.1:n.4482_4484del (ATM)
ENST00000527805.6:c.*3053_*3055del (ATM) ENSP00000435747.2:n.*3053_*3055del
ENST00000675595.1:c.*3124_*3126del (ATM) ENSP00000502563.1:n.*3124_*3126del
ENST00000675843.1:c.7989_7991del (ATM) MANE Select ENSP00000501606.1:p.Val2664del
ENST00000278616.8:c.7989_7991del (ATM) ENSP00000278616.4:p.Val2664del
ENST00000452508.6:c.7989_7991del (ATM) ENSP00000388058.2:p.Val2664del
ENST00000524755.5:c.299+1277_299+1279del (C11orf65)
ENST00000524792.5:n.4204_4206del (ATM)
ENST00000525056.1:n.186_188del (ATM)
ENST00000525729.5:c.641-24872_641-24870del (C11orf65) ENSP00000433395.1:n.641-24872_641-24870de...
ENST00000527531.5:c.*1269+1277_*1269+1279del (C11orf65) ENSP00000431706.1:n.*1269+1277_*1269+1279...
ENST00000533979.5:n.201_203del (ATM)
ENST00000615746.4:c.*1269+1277_*1269+1279del (C11orf65) ENSP00000483537.1:n.*1269+1277_*1269+1279...
NM_000051.3:c.7989_7991del , LRG_135t1:c.7989_7991del (ATM) NP_000042.3:p.Val2664del
XM_005271414.3:c.*38+1277_*38+1279del (C11orf65) XP_005271471.1:n.*38+1277_*38+1279del
XM_005271415.3:c.804+1277_804+1279del (C11orf65) XP_005271472.1:n.804+1277_804+1279del
XM_005271561.3:c.7989_7991del (ATM) XP_005271618.2:p.Val2664del
XM_005271562.3:c.7989_7991del (ATM) XP_005271619.2:p.Val2664del
XM_006718843.2:c.7989_7991del (ATM) XP_006718906.1:p.Val2664del
XM_006718845.1:c.3945_3947del (ATM) XP_006718908.1:p.Val1316del
XM_011542840.1:c.7989_7991del (ATM) XP_011541142.1:p.Val2664del
XM_011542841.1:c.7989_7991del (ATM) XP_011541143.1:p.Val2664del
XM_011542842.1:c.7824_7826del (ATM) XP_011541144.1:p.Val2609del
XM_011542843.1:c.7989_7991del (ATM) XP_011541145.1:p.Val2664del
XM_011542844.1:c.6945_6947del (ATM) XP_011541146.1:p.Val2316del
XM_011542845.1:c.6681_6683del (ATM) XP_011541147.1:p.Val2228del
XM_011542847.1:c.3060_3062del (ATM) XP_011541149.1:p.Val1021del
NM_001330368.1:c.641-24872_641-24870del (C11orf65) NP_001317297.1:n.641-24872_641-24870del
NM_001351110.1:c.*38+1277_*38+1279del (C11orf65) NP_001338039.1:n.*38+1277_*38+1279del
NM_001351834.1:c.7989_7991del (ATM) NP_001338763.1:p.Val2664del
NR_147053.2:n.2374+1277_2374+1279del (C11orf65)
XM_005271414.4:c.*38+1277_*38+1279del (C11orf65) XP_005271471.1:n.*38+1277_*38+1279del
XM_005271415.4:c.804+1277_804+1279del (C11orf65) XP_005271472.1:n.804+1277_804+1279del
XM_005271562.5:c.7989_7991del (ATM) XP_005271619.2:p.Val2664del
XM_006718843.4:c.7989_7991del (ATM) XP_006718906.1:p.Val2664del
XM_006718845.2:c.3945_3947del (ATM) XP_006718908.1:p.Val1316del
XM_011542840.3:c.7989_7991del (ATM) XP_011541142.1:p.Val2664del
XM_011542842.3:c.7824_7826del (ATM) XP_011541144.1:p.Val2609del
XM_011542843.2:c.7989_7991del (ATM) XP_011541145.1:p.Val2664del
XM_011542844.3:c.6945_6947del (ATM) XP_011541146.1:p.Val2316del
XM_011542845.2:c.6681_6683del (ATM) XP_011541147.1:p.Val2228del
XM_017017789.2:c.7989_7991del (ATM) XP_016873278.1:p.Val2664del
XM_017017790.2:c.7989_7991del (ATM) XP_016873279.1:p.Val2664del
NM_001330368.2:c.641-24872_641-24870del (C11orf65) NP_001317297.1:n.641-24872_641-24870del
NM_001351110.2:c.*38+1277_*38+1279del (C11orf65) NP_001338039.1:n.*38+1277_*38+1279del
NM_001351834.2:c.7989_7991del (ATM) NP_001338763.1:p.Val2664del
NM_000051.4:c.7989_7991del (ATM) MANE Select NP_000042.3:p.Val2664del
NR_147053.3:n.2372+1277_2372+1279del (C11orf65)