Canonical Allele Identifier: CA1407031578
Gene: ATR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142562379_142562380delinsCA , CM000665.2:g.142562379_142562380delinsCA GRCh38
NC_000003.11:g.142281221_142281222delinsCA , CM000665.1:g.142281221_142281222delinsCA GRCh37
NC_000003.10:g.143763911_143763912delinsCA NCBI36
NG_008951.1:g.21447_21448delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000350721.9:c.1022_1023delinsTG MANE Select ENSP00000343741.4:p.Leu341=
ENST00000515149.3:c.293-959_293-958delinsTG ENSP00000425897.3:n.293-959_293-958delinsTG
ENST00000653868.1:n.1051_1052delinsTG
ENST00000657914.1:n.3380_3381delinsTG
ENST00000659195.1:n.3087_3088delinsTG
ENST00000661310.1:c.1022_1023delinsTG ENSP00000499589.1:p.Leu341=
ENST00000350721.8:c.1022_1023delinsTG ENSP00000343741.4:p.Leu341=
ENST00000507148.1:c.293-32_293-31delinsTG ENSP00000426595.1:n.293-32_293-31delinsTG
ENST00000515149.2:c.65_66delinsTG ENSP00000425897.2:p.Leu22=
NM_001184.3:c.1022_1023delinsTG NP_001175.2:p.Leu341=
XM_011512924.1:c.1022_1023delinsTG XP_011511226.1:p.Leu341=
XM_011512925.1:c.1022_1023delinsTG XP_011511227.1:p.Leu341=
XM_011512926.1:c.1022_1023delinsTG XP_011511228.1:p.Leu341=
XM_011512927.1:c.1022_1023delinsTG XP_011511229.1:p.Leu341=
XR_924147.1:n.1111_1112delinsTG
XR_924148.1:n.1111_1112delinsTG
XR_924149.1:n.1111_1112delinsTG
NM_001354579.1:c.1022_1023delinsTG NP_001341508.1:p.Leu341=
XR_001740179.2:n.1111_1112delinsTG
XR_001740180.2:n.1111_1112delinsTG
XR_001740181.2:n.1111_1112delinsTG
XR_001740182.1:n.1111_1112delinsTG
XR_002959543.1:n.1111_1112delinsTG
XR_924148.2:n.1111_1112delinsTG
NM_001184.4:c.1022_1023delinsTG MANE Select NP_001175.2:p.Leu341=
NM_001354579.2:c.1022_1023delinsTG NP_001341508.1:p.Leu341=