Canonical Allele Identifier: CA382551205

Gene: ATM C11orf65

Linked Data

• dbSNP Id: rs1064795467
• gnomAD v2: 11-108188139-T-C
• gnomAD v4: 11-108317412-T-C
• MyVariant Identifiers: chr11:g.108188139T>C (hg19) ; chr11:g.108317412T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108317412T>C , CM000673.2:g.108317412T>C	GRCh38
NC_000011.9:g.108188139T>C , CM000673.1:g.108188139T>C	GRCh37
NC_000011.8:g.107693349T>C	NCBI36
NG_009830.1:g.99581T>C , LRG_135:g.99581T>C
NG_054724.1:g.157421A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000452508.7:c.6238T>C (ATM)	ENSP00000388058.2:p.Tyr2080His
ENST00000713593.1:c.*5709T>C (ATM)	ENSP00000518889.1:n.*5709T>C
ENST00000278616.9:c.6238T>C (ATM)	ENSP00000278616.4:p.Tyr2080His
ENST00000525056.2:n.657T>C (ATM)
ENST00000682286.1:n.995T>C (ATM)
ENST00000682302.1:n.656T>C (ATM)
ENST00000683174.1:n.7722T>C (ATM)
ENST00000683524.1:n.1462T>C (ATM)
ENST00000684152.1:n.1952T>C (ATM)
ENST00000527805.6:c.*1302T>C (ATM)	ENSP00000435747.2:n.*1302T>C
ENST00000675595.1:c.*1302T>C (ATM)	ENSP00000502563.1:n.*1302T>C
ENST00000675843.1:c.6238T>C (ATM) MANE Select	ENSP00000501606.1:p.Tyr2080His
ENST00000278616.8:c.6238T>C (ATM)	ENSP00000278616.4:p.Tyr2080His
ENST00000452508.6:c.6238T>C (ATM)	ENSP00000388058.2:p.Tyr2080His
ENST00000524792.5:n.2453T>C (ATM)
ENST00000525729.5:c.641-8341A>G (C11orf65)	ENSP00000433395.1:n.641-8341A>G
ENST00000532765.1:n.555T>C (ATM)
ENST00000533690.5:n.1642T>C (ATM)
NM_000051.3:c.6238T>C , LRG_135t1:c.6238T>C (ATM)	NP_000042.3:p.Tyr2080His
XM_005271561.3:c.6238T>C (ATM)	XP_005271618.2:p.Tyr2080His
XM_005271562.3:c.6238T>C (ATM)	XP_005271619.2:p.Tyr2080His
XM_006718843.2:c.6238T>C (ATM)	XP_006718906.1:p.Tyr2080His
XM_006718845.1:c.2194T>C (ATM)	XP_006718908.1:p.Tyr732His
XM_011542840.1:c.6238T>C (ATM)	XP_011541142.1:p.Tyr2080His
XM_011542841.1:c.6238T>C (ATM)	XP_011541143.1:p.Tyr2080His
XM_011542842.1:c.6073T>C (ATM)	XP_011541144.1:p.Tyr2025His
XM_011542843.1:c.6238T>C (ATM)	XP_011541145.1:p.Tyr2080His
XM_011542844.1:c.5194T>C (ATM)	XP_011541146.1:p.Tyr1732His
XM_011542845.1:c.4930T>C (ATM)	XP_011541147.1:p.Tyr1644His
XM_011542847.1:c.1309T>C (ATM)	XP_011541149.1:p.Tyr437His
NM_001330368.1:c.641-8341A>G (C11orf65)	NP_001317297.1:n.641-8341A>G
NM_001351110.1:c.*39-8341A>G (C11orf65)	NP_001338039.1:n.*39-8341A>G
NM_001351834.1:c.6238T>C (ATM)	NP_001338763.1:p.Tyr2080His
XM_005271562.5:c.6238T>C (ATM)	XP_005271619.2:p.Tyr2080His
XM_006718843.4:c.6238T>C (ATM)	XP_006718906.1:p.Tyr2080His
XM_006718845.2:c.2194T>C (ATM)	XP_006718908.1:p.Tyr732His
XM_011542840.3:c.6238T>C (ATM)	XP_011541142.1:p.Tyr2080His
XM_011542842.3:c.6073T>C (ATM)	XP_011541144.1:p.Tyr2025His
XM_011542843.2:c.6238T>C (ATM)	XP_011541145.1:p.Tyr2080His
XM_011542844.3:c.5194T>C (ATM)	XP_011541146.1:p.Tyr1732His
XM_011542845.2:c.4930T>C (ATM)	XP_011541147.1:p.Tyr1644His
XM_017017789.2:c.6238T>C (ATM)	XP_016873278.1:p.Tyr2080His
XM_017017790.2:c.6238T>C (ATM)	XP_016873279.1:p.Tyr2080His
XM_017017791.1:c.6238T>C (ATM)	XP_016873280.1:p.Tyr2080His
NM_001330368.2:c.641-8341A>G (C11orf65)	NP_001317297.1:n.641-8341A>G
NM_001351110.2:c.*39-8341A>G (C11orf65)	NP_001338039.1:n.*39-8341A>G
NM_001351834.2:c.6238T>C (ATM)	NP_001338763.1:p.Tyr2080His
NM_000051.4:c.6238T>C (ATM) MANE Select	NP_000042.3:p.Tyr2080His