Canonical Allele Identifier: CA1407028951

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142553216_142553217delinsCT , CM000665.2:g.142553216_142553217delinsCT	GRCh38
NC_000003.11:g.142272058_142272059delinsCT , CM000665.1:g.142272058_142272059delinsCT	GRCh37
NC_000003.10:g.143754748_143754749delinsCT	NCBI36
NG_008951.1:g.30610_30611delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.2805+10_2805+11delinsAG MANE Select	ENSP00000343741.4:n.2805+10_2805+11delinsAG
ENST00000515149.3:c.*1579+10_*1579+11delinsAG	ENSP00000425897.3:n.*1579+10_*1579+11delinsAG
ENST00000653868.1:n.2834+10_2834+11delinsAG
ENST00000656582.1:n.64+10_64+11delinsAG
ENST00000656590.1:c.1595+10_1595+11delinsAG
ENST00000659195.1:n.5680+10_5680+11delinsAG
ENST00000661310.1:c.2613+10_2613+11delinsAG	ENSP00000499589.1:n.2613+10_2613+11delinsAG
ENST00000350721.8:c.2805+10_2805+11delinsAG	ENSP00000343741.4:n.2805+10_2805+11delinsAG
NM_001184.3:c.2805+10_2805+11delinsAG	NP_001175.2:n.2805+10_2805+11delinsAG
XM_011512924.1:c.2805+10_2805+11delinsAG	XP_011511226.1:n.2805+10_2805+11delinsAG
XM_011512925.1:c.2613+10_2613+11delinsAG	XP_011511227.1:n.2613+10_2613+11delinsAG
XM_011512926.1:c.2805+10_2805+11delinsAG	XP_011511228.1:n.2805+10_2805+11delinsAG
XM_011512927.1:c.2805+10_2805+11delinsAG	XP_011511229.1:n.2805+10_2805+11delinsAG
XR_924147.1:n.2894+10_2894+11delinsAG
XR_924148.1:n.2894+10_2894+11delinsAG
XR_924149.1:n.2894+10_2894+11delinsAG
NM_001354579.1:c.2613+10_2613+11delinsAG	NP_001341508.1:n.2613+10_2613+11delinsAG
XR_001740179.2:n.2894+10_2894+11delinsAG
XR_001740180.2:n.2894+10_2894+11delinsAG
XR_001740181.2:n.2894+10_2894+11delinsAG
XR_001740182.1:n.2894+10_2894+11delinsAG
XR_002959543.1:n.2894+10_2894+11delinsAG
XR_924148.2:n.2894+10_2894+11delinsAG
NM_001184.4:c.2805+10_2805+11delinsAG MANE Select	NP_001175.2:n.2805+10_2805+11delinsAG
NM_001354579.2:c.2613+10_2613+11delinsAG	NP_001341508.1:n.2613+10_2613+11delinsAG