Canonical Allele Identifier: CA1407031827

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142563129_142563131delinsGAT , CM000665.2:g.142563129_142563131delinsGAT	GRCh38
NC_000003.11:g.142281971_142281973delinsGAT , CM000665.1:g.142281971_142281973delinsGAT	GRCh37
NC_000003.10:g.143764661_143764663delinsGAT	NCBI36
NG_008951.1:g.20696_20698delinsATC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.293-22_293-20delinsATC MANE Select	ENSP00000343741.4:n.293-22_293-20delinsATC
ENST00000515149.3:c.293-1710_293-1708delinsATC	ENSP00000425897.3:n.293-1710_293-1708delinsATC
ENST00000653868.1:n.322-22_322-20delinsATC
ENST00000657914.1:n.2629_2631delinsATC
ENST00000659195.1:n.2336_2338delinsATC
ENST00000661310.1:c.293-22_293-20delinsATC	ENSP00000499589.1:n.293-22_293-20delinsATC
ENST00000350721.8:c.293-22_293-20delinsATC	ENSP00000343741.4:n.293-22_293-20delinsATC
ENST00000507148.1:c.293-783_293-781delinsATC	ENSP00000426595.1:n.293-783_293-781delinsATC
NM_001184.3:c.293-22_293-20delinsATC	NP_001175.2:n.293-22_293-20delinsATC
XM_011512924.1:c.293-22_293-20delinsATC	XP_011511226.1:n.293-22_293-20delinsATC
XM_011512925.1:c.293-22_293-20delinsATC	XP_011511227.1:n.293-22_293-20delinsATC
XM_011512926.1:c.293-22_293-20delinsATC	XP_011511228.1:n.293-22_293-20delinsATC
XM_011512927.1:c.293-22_293-20delinsATC	XP_011511229.1:n.293-22_293-20delinsATC
XR_924147.1:n.382-22_382-20delinsATC
XR_924148.1:n.382-22_382-20delinsATC
XR_924149.1:n.382-22_382-20delinsATC
NM_001354579.1:c.293-22_293-20delinsATC	NP_001341508.1:n.293-22_293-20delinsATC
XR_001740179.2:n.382-22_382-20delinsATC
XR_001740180.2:n.382-22_382-20delinsATC
XR_001740181.2:n.382-22_382-20delinsATC
XR_001740182.1:n.382-22_382-20delinsATC
XR_002959543.1:n.382-22_382-20delinsATC
XR_924148.2:n.382-22_382-20delinsATC
NM_001184.4:c.293-22_293-20delinsATC MANE Select	NP_001175.2:n.293-22_293-20delinsATC
NM_001354579.2:c.293-22_293-20delinsATC	NP_001341508.1:n.293-22_293-20delinsATC