Canonical Allele Identifier: CA2615856658

Gene: ATM

Linked Data

• gnomAD v4: 11-108243933-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108243933_108243934insG , CM000673.2:g.108243933_108243934insG	GRCh38
NC_000011.9:g.108114660_108114661insG , CM000673.1:g.108114660_108114661insG	GRCh37
NC_000011.8:g.107619870_107619871insG	NCBI36
NG_009830.1:g.26102_26103insG , LRG_135:g.26102_26103insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452508.7:c.497-20_497-19insG	ENSP00000388058.2:n.497-20_497-19insG
ENST00000713593.1:c.497-42_497-41insG	ENSP00000518889.1:n.497-42_497-41insG
ENST00000278616.9:c.497-20_497-19insG	ENSP00000278616.4:n.497-20_497-19insG
ENST00000682430.1:n.596-20_596-19insG
ENST00000682516.1:n.631-20_631-19insG
ENST00000682956.1:n.631-20_631-19insG
ENST00000683100.1:n.2155_2156insG
ENST00000683174.1:n.647-20_647-19insG
ENST00000684037.1:c.497-20_497-19insG	ENSP00000508245.1:n.497-20_497-19insG
ENST00000684061.1:n.631-20_631-19insG
ENST00000684179.1:n.466-20_466-19insG
ENST00000527805.6:c.497-20_497-19insG	ENSP00000435747.2:n.497-20_497-19insG
ENST00000675595.1:c.332-20_332-19insG	ENSP00000502563.1:n.332-20_332-19insG
ENST00000675843.1:c.497-20_497-19insG MANE Select	ENSP00000501606.1:n.497-20_497-19insG
ENST00000278616.8:c.497-20_497-19insG	ENSP00000278616.4:n.497-20_497-19insG
ENST00000452508.6:c.497-20_497-19insG	ENSP00000388058.2:n.497-20_497-19insG
ENST00000527805.5:c.497-20_497-19insG	ENSP00000435747.1:n.497-20_497-19insG
ENST00000527891.5:c.332-20_332-19insG	ENSP00000433955.1:n.332-20_332-19insG
NM_000051.3:c.497-20_497-19insG , LRG_135t1:c.497-20_497-19insG	NP_000042.3:n.497-20_497-19insG
XM_005271561.3:c.497-20_497-19insG	XP_005271618.2:n.497-20_497-19insG
XM_005271562.3:c.497-20_497-19insG	XP_005271619.2:n.497-20_497-19insG
XM_006718843.2:c.497-20_497-19insG	XP_006718906.1:n.497-20_497-19insG
XM_011542840.1:c.497-20_497-19insG	XP_011541142.1:n.497-20_497-19insG
XM_011542841.1:c.497-20_497-19insG	XP_011541143.1:n.497-20_497-19insG
XM_011542842.1:c.332-20_332-19insG	XP_011541144.1:n.332-20_332-19insG
XM_011542843.1:c.497-20_497-19insG	XP_011541145.1:n.497-20_497-19insG
XM_011542844.1:c.-526-42_-526-41insG	XP_011541146.1:n.-526-42_-526-41insG
XM_011542846.1:c.497-20_497-19insG	XP_011541148.1:n.497-20_497-19insG
NM_001351834.1:c.497-20_497-19insG	NP_001338763.1:n.497-20_497-19insG
XM_005271562.5:c.497-20_497-19insG	XP_005271619.2:n.497-20_497-19insG
XM_006718843.4:c.497-20_497-19insG	XP_006718906.1:n.497-20_497-19insG
XM_011542840.3:c.497-20_497-19insG	XP_011541142.1:n.497-20_497-19insG
XM_011542842.3:c.332-20_332-19insG	XP_011541144.1:n.332-20_332-19insG
XM_011542843.2:c.497-20_497-19insG	XP_011541145.1:n.497-20_497-19insG
XM_011542844.3:c.-526-42_-526-41insG	XP_011541146.1:n.-526-42_-526-41insG
XM_017017789.2:c.497-20_497-19insG	XP_016873278.1:n.497-20_497-19insG
XM_017017790.2:c.497-20_497-19insG	XP_016873279.1:n.497-20_497-19insG
XM_017017791.1:c.497-20_497-19insG	XP_016873280.1:n.497-20_497-19insG
XM_017017792.2:c.497-20_497-19insG	XP_016873281.1:n.497-20_497-19insG
XR_002957150.1:n.1230-20_1230-19insG
NM_001351834.2:c.497-20_497-19insG	NP_001338763.1:n.497-20_497-19insG
NM_000051.4:c.497-20_497-19insG MANE Select	NP_000042.3:n.497-20_497-19insG