Canonical Allele Identifier: CA2577924877

Gene: ATR

Linked Data

• gnomAD v4: 3-142470086-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470091del , CM000665.2:g.142470091del	GRCh38
NC_000003.11:g.142188933del , CM000665.1:g.142188933del	GRCh37
NC_000003.10:g.143671623del	NCBI36
NG_008951.1:g.113740del

Transcript Alleles

HGVS	Amino-acid change
ENST00000350721.9:c.6318del MANE Select	ENSP00000343741.4:p.Ala2107LeufsTer9
ENST00000513291.2:n.1502del
ENST00000654170.1:n.1161del
ENST00000656590.1:c.5108del
ENST00000661310.1:c.6126del	ENSP00000499589.1:p.Ala2043LeufsTer9
ENST00000665483.1:n.173del
ENST00000666447.1:n.153del
ENST00000666943.1:n.1782del
ENST00000350721.8:c.6318del	ENSP00000343741.4:p.Ala2107LeufsTer9
NM_001184.3:c.6318del	NP_001175.2:p.Ala2107LeufsTer9
XM_011512924.1:c.6324del	XP_011511226.1:p.Ala2109LeufsTer9
XM_011512925.1:c.6132del	XP_011511227.1:p.Ala2045LeufsTer9
XR_924147.1:n.6413del
XR_924148.1:n.6413del
XR_924149.1:n.6292del
NM_001354579.1:c.6126del	NP_001341508.1:p.Ala2043LeufsTer9
XR_001740179.2:n.6407del
XR_001740180.2:n.6461del
XR_001740181.2:n.6340del
XR_001740182.1:n.6292del
XR_002959543.1:n.6517del
XR_924148.2:n.6413del
NM_001184.4:c.6318del MANE Select	NP_001175.2:p.Ala2107LeufsTer9
NM_001354579.2:c.6126del	NP_001341508.1:p.Ala2043LeufsTer9