Canonical Allele Identifier: CA2668042798

Gene: ATR

Linked Data

• gnomAD v4: 3-142563138-TAAAC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142563141_142563144del , CM000665.2:g.142563141_142563144del	GRCh38
NC_000003.11:g.142281983_142281986del , CM000665.1:g.142281983_142281986del	GRCh37
NC_000003.10:g.143764673_143764676del	NCBI36
NG_008951.1:g.20685_20688del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.293-33_293-30del MANE Select	ENSP00000343741.4:n.293-33_293-30del
ENST00000515149.3:c.293-1721_293-1718del	ENSP00000425897.3:n.293-1721_293-1718del
ENST00000653868.1:n.322-33_322-30del
ENST00000657914.1:n.2618_2621del
ENST00000659195.1:n.2325_2328del
ENST00000661310.1:c.293-33_293-30del	ENSP00000499589.1:n.293-33_293-30del
ENST00000350721.8:c.293-33_293-30del	ENSP00000343741.4:n.293-33_293-30del
ENST00000507148.1:c.293-794_293-791del	ENSP00000426595.1:n.293-794_293-791del
NM_001184.3:c.293-33_293-30del	NP_001175.2:n.293-33_293-30del
XM_011512924.1:c.293-33_293-30del	XP_011511226.1:n.293-33_293-30del
XM_011512925.1:c.293-33_293-30del	XP_011511227.1:n.293-33_293-30del
XM_011512926.1:c.293-33_293-30del	XP_011511228.1:n.293-33_293-30del
XM_011512927.1:c.293-33_293-30del	XP_011511229.1:n.293-33_293-30del
XR_924147.1:n.382-33_382-30del
XR_924148.1:n.382-33_382-30del
XR_924149.1:n.382-33_382-30del
NM_001354579.1:c.293-33_293-30del	NP_001341508.1:n.293-33_293-30del
XR_001740179.2:n.382-33_382-30del
XR_001740180.2:n.382-33_382-30del
XR_001740181.2:n.382-33_382-30del
XR_001740182.1:n.382-33_382-30del
XR_002959543.1:n.382-33_382-30del
XR_924148.2:n.382-33_382-30del
NM_001184.4:c.293-33_293-30del MANE Select	NP_001175.2:n.293-33_293-30del
NM_001354579.2:c.293-33_293-30del	NP_001341508.1:n.293-33_293-30del