Canonical Allele Identifier: CA1407031792

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142563006_142563009delinsAAAT , CM000665.2:g.142563006_142563009delinsAAAT	GRCh38
NC_000003.11:g.142281848_142281851delinsAAAT , CM000665.1:g.142281848_142281851delinsAAAT	GRCh37
NC_000003.10:g.143764538_143764541delinsAAAT	NCBI36
NG_008951.1:g.20818_20821delinsATTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.393_396delinsATTT MANE Select	ENSP00000343741.4:p.Leu131=
ENST00000515149.3:c.293-1588_293-1585delinsATTT	ENSP00000425897.3:n.293-1588_293-1585delinsATTT
ENST00000653868.1:n.422_425delinsATTT
ENST00000657914.1:n.2751_2754delinsATTT
ENST00000659195.1:n.2458_2461delinsATTT
ENST00000661310.1:c.393_396delinsATTT	ENSP00000499589.1:p.Leu131=
ENST00000350721.8:c.393_396delinsATTT	ENSP00000343741.4:p.Leu131=
ENST00000507148.1:c.293-661_293-658delinsATTT	ENSP00000426595.1:n.293-661_293-658delinsATTT
NM_001184.3:c.393_396delinsATTT	NP_001175.2:p.Leu131=
XM_011512924.1:c.393_396delinsATTT	XP_011511226.1:p.Leu131=
XM_011512925.1:c.393_396delinsATTT	XP_011511227.1:p.Leu131=
XM_011512926.1:c.393_396delinsATTT	XP_011511228.1:p.Leu131=
XM_011512927.1:c.393_396delinsATTT	XP_011511229.1:p.Leu131=
XR_924147.1:n.482_485delinsATTT
XR_924148.1:n.482_485delinsATTT
XR_924149.1:n.482_485delinsATTT
NM_001354579.1:c.393_396delinsATTT	NP_001341508.1:p.Leu131=
XR_001740179.2:n.482_485delinsATTT
XR_001740180.2:n.482_485delinsATTT
XR_001740181.2:n.482_485delinsATTT
XR_001740182.1:n.482_485delinsATTT
XR_002959543.1:n.482_485delinsATTT
XR_924148.2:n.482_485delinsATTT
NM_001184.4:c.393_396delinsATTT MANE Select	NP_001175.2:p.Leu131=
NM_001354579.2:c.393_396delinsATTT	NP_001341508.1:p.Leu131=