Canonical Allele Identifier: CA382534043

Gene: ATM

Linked Data

• ClinVar Variation Id: 482694
• ClinVar RCV Id: RCV000574447 ; RCV000697193 ; RCV001357554 ; RCV003465228
• dbSNP Id: rs1555070941
• gnomAD v4: 11-108250896-G-C
• MyVariant Identifiers: chr11:g.108121623G>C (hg19) ; chr11:g.108250896G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108250896G>C , CM000673.2:g.108250896G>C	GRCh38
NC_000011.9:g.108121623G>C , CM000673.1:g.108121623G>C	GRCh37
NC_000011.8:g.107626833G>C	NCBI36
NG_009830.1:g.33065G>C , LRG_135:g.33065G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000452508.7:c.1431G>C	ENSP00000388058.2:p.Lys477Asn
ENST00000713593.1:c.*902G>C	ENSP00000518889.1:n.*902G>C
ENST00000278616.9:c.1431G>C	ENSP00000278616.4:p.Lys477Asn
ENST00000682516.1:n.1565G>C
ENST00000682956.1:n.1565G>C
ENST00000683174.1:n.1581G>C
ENST00000683605.1:n.926G>C
ENST00000684037.1:c.*366G>C	ENSP00000508245.1:n.*366G>C
ENST00000684061.1:n.1565G>C
ENST00000684179.1:n.1400G>C
ENST00000527805.6:c.1431G>C	ENSP00000435747.2:p.Lys477Asn
ENST00000675595.1:c.1266G>C	ENSP00000502563.1:p.Lys422Asn
ENST00000675843.1:c.1431G>C MANE Select	ENSP00000501606.1:p.Lys477Asn
ENST00000278616.8:c.1431G>C	ENSP00000278616.4:p.Lys477Asn
ENST00000452508.6:c.1431G>C	ENSP00000388058.2:p.Lys477Asn
ENST00000527805.5:c.1431G>C	ENSP00000435747.1:p.Lys477Asn
NM_000051.3:c.1431G>C , LRG_135t1:c.1431G>C	NP_000042.3:p.Lys477Asn
XM_005271561.3:c.1431G>C	XP_005271618.2:p.Lys477Asn
XM_005271562.3:c.1431G>C	XP_005271619.2:p.Lys477Asn
XM_006718843.2:c.1431G>C	XP_006718906.1:p.Lys477Asn
XM_011542840.1:c.1431G>C	XP_011541142.1:p.Lys477Asn
XM_011542841.1:c.1431G>C	XP_011541143.1:p.Lys477Asn
XM_011542842.1:c.1266G>C	XP_011541144.1:p.Lys422Asn
XM_011542843.1:c.1431G>C	XP_011541145.1:p.Lys477Asn
XM_011542844.1:c.387G>C	XP_011541146.1:p.Lys129Asn
XM_011542845.1:c.123G>C	XP_011541147.1:p.Lys41Asn
XM_011542846.1:c.1431G>C	XP_011541148.1:p.Lys477Asn
NM_001351834.1:c.1431G>C	NP_001338763.1:p.Lys477Asn
XM_005271562.5:c.1431G>C	XP_005271619.2:p.Lys477Asn
XM_006718843.4:c.1431G>C	XP_006718906.1:p.Lys477Asn
XM_011542840.3:c.1431G>C	XP_011541142.1:p.Lys477Asn
XM_011542842.3:c.1266G>C	XP_011541144.1:p.Lys422Asn
XM_011542843.2:c.1431G>C	XP_011541145.1:p.Lys477Asn
XM_011542844.3:c.387G>C	XP_011541146.1:p.Lys129Asn
XM_011542845.2:c.123G>C	XP_011541147.1:p.Lys41Asn
XM_017017789.2:c.1431G>C	XP_016873278.1:p.Lys477Asn
XM_017017790.2:c.1431G>C	XP_016873279.1:p.Lys477Asn
XM_017017791.1:c.1431G>C	XP_016873280.1:p.Lys477Asn
XM_017017792.2:c.1431G>C	XP_016873281.1:p.Lys477Asn
XR_002957150.1:n.2164G>C
NM_001351834.2:c.1431G>C	NP_001338763.1:p.Lys477Asn
NM_000051.4:c.1431G>C MANE Select	NP_000042.3:p.Lys477Asn