Canonical Allele Identifier: CA2615859379

Gene: ATM C11orf65

Linked Data

• gnomAD v4: 11-108315968-TGTGTGTAAAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108315969_108315978del , CM000673.2:g.108315969_108315978del	GRCh38
NC_000011.9:g.108186696_108186705del , CM000673.1:g.108186696_108186705del	GRCh37
NC_000011.8:g.107691906_107691915del	NCBI36
NG_009830.1:g.98138_98147del , LRG_135:g.98138_98147del
NG_054724.1:g.158855_158864del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.6096-42_6096-33del (ATM)	ENSP00000388058.2:n.6096-42_6096-33del
ENST00000713593.1:c.*5567-42_*5567-33del (ATM)	ENSP00000518889.1:n.*5567-42_*5567-33del
ENST00000278616.9:c.6096-42_6096-33del (ATM)	ENSP00000278616.4:n.6096-42_6096-33del
ENST00000525056.2:n.515-42_515-33del (ATM)
ENST00000682286.1:n.853-42_853-33del (ATM)
ENST00000682302.1:n.514-42_514-33del (ATM)
ENST00000683174.1:n.7580-42_7580-33del (ATM)
ENST00000683524.1:n.1320-42_1320-33del (ATM)
ENST00000684152.1:n.1810-42_1810-33del (ATM)
ENST00000527805.6:c.*1160-42_*1160-33del (ATM)	ENSP00000435747.2:n.*1160-42_*1160-33del
ENST00000675595.1:c.*1160-42_*1160-33del (ATM)	ENSP00000502563.1:n.*1160-42_*1160-33del
ENST00000675843.1:c.6096-42_6096-33del (ATM) MANE Select	ENSP00000501606.1:n.6096-42_6096-33del
ENST00000278616.8:c.6096-42_6096-33del (ATM)	ENSP00000278616.4:n.6096-42_6096-33del
ENST00000452508.6:c.6096-42_6096-33del (ATM)	ENSP00000388058.2:n.6096-42_6096-33del
ENST00000524792.5:n.2311-42_2311-33del (ATM)
ENST00000525729.5:c.641-6907_641-6898del (C11orf65)	ENSP00000433395.1:n.641-6907_641-6898del
ENST00000532765.1:n.413-42_413-33del (ATM)
ENST00000533690.5:n.1500-42_1500-33del (ATM)
NM_000051.3:c.6096-42_6096-33del , LRG_135t1:c.6096-42_6096-33del (ATM)	NP_000042.3:n.6096-42_6096-33del
XM_005271561.3:c.6096-42_6096-33del (ATM)	XP_005271618.2:n.6096-42_6096-33del
XM_005271562.3:c.6096-42_6096-33del (ATM)	XP_005271619.2:n.6096-42_6096-33del
XM_006718843.2:c.6096-42_6096-33del (ATM)	XP_006718906.1:n.6096-42_6096-33del
XM_006718845.1:c.2052-42_2052-33del (ATM)	XP_006718908.1:n.2052-42_2052-33del
XM_011542840.1:c.6096-42_6096-33del (ATM)	XP_011541142.1:n.6096-42_6096-33del
XM_011542841.1:c.6096-42_6096-33del (ATM)	XP_011541143.1:n.6096-42_6096-33del
XM_011542842.1:c.5931-42_5931-33del (ATM)	XP_011541144.1:n.5931-42_5931-33del
XM_011542843.1:c.6096-42_6096-33del (ATM)	XP_011541145.1:n.6096-42_6096-33del
XM_011542844.1:c.5052-42_5052-33del (ATM)	XP_011541146.1:n.5052-42_5052-33del
XM_011542845.1:c.4788-42_4788-33del (ATM)	XP_011541147.1:n.4788-42_4788-33del
XM_011542847.1:c.1167-42_1167-33del (ATM)	XP_011541149.1:n.1167-42_1167-33del
NM_001330368.1:c.641-6907_641-6898del (C11orf65)	NP_001317297.1:n.641-6907_641-6898del
NM_001351110.1:c.*39-6907_*39-6898del (C11orf65)	NP_001338039.1:n.*39-6907_*39-6898del
NM_001351834.1:c.6096-42_6096-33del (ATM)	NP_001338763.1:n.6096-42_6096-33del
XM_005271562.5:c.6096-42_6096-33del (ATM)	XP_005271619.2:n.6096-42_6096-33del
XM_006718843.4:c.6096-42_6096-33del (ATM)	XP_006718906.1:n.6096-42_6096-33del
XM_006718845.2:c.2052-42_2052-33del (ATM)	XP_006718908.1:n.2052-42_2052-33del
XM_011542840.3:c.6096-42_6096-33del (ATM)	XP_011541142.1:n.6096-42_6096-33del
XM_011542842.3:c.5931-42_5931-33del (ATM)	XP_011541144.1:n.5931-42_5931-33del
XM_011542843.2:c.6096-42_6096-33del (ATM)	XP_011541145.1:n.6096-42_6096-33del
XM_011542844.3:c.5052-42_5052-33del (ATM)	XP_011541146.1:n.5052-42_5052-33del
XM_011542845.2:c.4788-42_4788-33del (ATM)	XP_011541147.1:n.4788-42_4788-33del
XM_017017789.2:c.6096-42_6096-33del (ATM)	XP_016873278.1:n.6096-42_6096-33del
XM_017017790.2:c.6096-42_6096-33del (ATM)	XP_016873279.1:n.6096-42_6096-33del
XM_017017791.1:c.6096-42_6096-33del (ATM)	XP_016873280.1:n.6096-42_6096-33del
NM_001330368.2:c.641-6907_641-6898del (C11orf65)	NP_001317297.1:n.641-6907_641-6898del
NM_001351110.2:c.*39-6907_*39-6898del (C11orf65)	NP_001338039.1:n.*39-6907_*39-6898del
NM_001351834.2:c.6096-42_6096-33del (ATM)	NP_001338763.1:n.6096-42_6096-33del
NM_000051.4:c.6096-42_6096-33del (ATM) MANE Select	NP_000042.3:n.6096-42_6096-33del