Canonical Allele Identifier: CA658656244

Gene: ATM

Linked Data

• ClinVar Variation Id: 482640
• ClinVar RCV Id: RCV000564979
• dbSNP Id: rs1555082344
• MyVariant Identifiers: chr11:g.108138055del (hg19) ; chr11:g.108267328del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108267328del , CM000673.2:g.108267328del	GRCh38
NC_000011.9:g.108138055del , CM000673.1:g.108138055del	GRCh37
NC_000011.8:g.107643265del	NCBI36
NG_009830.1:g.49497del , LRG_135:g.49497del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.2624del	ENSP00000388058.2:p.Ser875ThrfsTer5
ENST00000713593.1:c.*2095del	ENSP00000518889.1:n.*2095del
ENST00000278616.9:c.2624del	ENSP00000278616.4:p.Ser875ThrfsTer5
ENST00000682516.1:n.2758del
ENST00000683174.1:n.2774del
ENST00000683605.1:n.2119del
ENST00000684037.1:c.*1559del	ENSP00000508245.1:n.*1559del
ENST00000527805.6:c.2624del	ENSP00000435747.2:p.Ser875ThrfsTer5
ENST00000675595.1:c.2459del	ENSP00000502563.1:p.Ser820ThrfsTer5
ENST00000675843.1:c.2624del MANE Select	ENSP00000501606.1:p.Ser875ThrfsTer5
ENST00000278616.8:c.2624del	ENSP00000278616.4:p.Ser875ThrfsTer5
ENST00000452508.6:c.2624del	ENSP00000388058.2:p.Ser875ThrfsTer5
ENST00000527805.5:c.2624del	ENSP00000435747.1:p.Ser875ThrfsTer5
NM_000051.3:c.2624del , LRG_135t1:c.2624del	NP_000042.3:p.Ser875ThrfsTer5
XM_005271561.3:c.2624del	XP_005271618.2:p.Ser875ThrfsTer5
XM_005271562.3:c.2624del	XP_005271619.2:p.Ser875ThrfsTer5
XM_006718843.2:c.2624del	XP_006718906.1:p.Ser875ThrfsTer5
XM_011542840.1:c.2624del	XP_011541142.1:p.Ser875ThrfsTer5
XM_011542841.1:c.2624del	XP_011541143.1:p.Ser875ThrfsTer5
XM_011542842.1:c.2459del	XP_011541144.1:p.Ser820ThrfsTer5
XM_011542843.1:c.2624del	XP_011541145.1:p.Ser875ThrfsTer5
XM_011542844.1:c.1580del	XP_011541146.1:p.Ser527ThrfsTer5
XM_011542845.1:c.1316del	XP_011541147.1:p.Ser439ThrfsTer5
XM_011542846.1:c.2624del	XP_011541148.1:p.Ser875ThrfsTer5
NM_001351834.1:c.2624del	NP_001338763.1:p.Ser875ThrfsTer5
XM_005271562.5:c.2624del	XP_005271619.2:p.Ser875ThrfsTer5
XM_006718843.4:c.2624del	XP_006718906.1:p.Ser875ThrfsTer5
XM_011542840.3:c.2624del	XP_011541142.1:p.Ser875ThrfsTer5
XM_011542842.3:c.2459del	XP_011541144.1:p.Ser820ThrfsTer5
XM_011542843.2:c.2624del	XP_011541145.1:p.Ser875ThrfsTer5
XM_011542844.3:c.1580del	XP_011541146.1:p.Ser527ThrfsTer5
XM_011542845.2:c.1316del	XP_011541147.1:p.Ser439ThrfsTer5
XM_017017789.2:c.2624del	XP_016873278.1:p.Ser875ThrfsTer5
XM_017017790.2:c.2624del	XP_016873279.1:p.Ser875ThrfsTer5
XM_017017791.1:c.2624del	XP_016873280.1:p.Ser875ThrfsTer5
XM_017017792.2:c.2624del	XP_016873281.1:p.Ser875ThrfsTer5
XR_002957150.1:n.3357del
NM_001351834.2:c.2624del	NP_001338763.1:p.Ser875ThrfsTer5
NM_000051.4:c.2624del MANE Select	NP_000042.3:p.Ser875ThrfsTer5