Canonical Allele Identifier: CA2577925519

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142553653del , CM000665.2:g.142553653del	GRCh38
NC_000003.11:g.142272495del , CM000665.1:g.142272495del	GRCh37
NC_000003.10:g.143755185del	NCBI36
NG_008951.1:g.30177del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.2623del MANE Select	ENSP00000343741.4:p.Asp875IlefsTer?
ENST00000515149.3:c.*1397del	ENSP00000425897.3:n.*1397del
ENST00000653868.1:n.2652del
ENST00000656590.1:c.1413del
ENST00000659195.1:n.5498del
ENST00000661310.1:c.2431del	ENSP00000499589.1:p.Asp811IlefsTer?
ENST00000350721.8:c.2623del	ENSP00000343741.4:p.Asp875IlefsTer?
NM_001184.3:c.2623del	NP_001175.2:p.Asp875IlefsTer?
XM_011512924.1:c.2623del	XP_011511226.1:p.Asp875IlefsTer?
XM_011512925.1:c.2431del	XP_011511227.1:p.Asp811IlefsTer?
XM_011512926.1:c.2623del	XP_011511228.1:p.Asp875IlefsTer?
XM_011512927.1:c.2623del	XP_011511229.1:p.Asp875IlefsTer?
XR_924147.1:n.2712del
XR_924148.1:n.2712del
XR_924149.1:n.2712del
NM_001354579.1:c.2431del	NP_001341508.1:p.Asp811IlefsTer?
XR_001740179.2:n.2712del
XR_001740180.2:n.2712del
XR_001740181.2:n.2712del
XR_001740182.1:n.2712del
XR_002959543.1:n.2712del
XR_924148.2:n.2712del
NM_001184.4:c.2623del MANE Select	NP_001175.2:p.Asp875IlefsTer?
NM_001354579.2:c.2431del	NP_001341508.1:p.Asp811IlefsTer?