Canonical Allele Identifier: CA645523890
Gene: ATR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142562591_142562592insA , CM000665.2:g.142562591_142562592insA GRCh38
NC_000003.11:g.142281433_142281434insA , CM000665.1:g.142281433_142281434insA GRCh37
NC_000003.10:g.143764123_143764124insA NCBI36
NG_008951.1:g.21235_21236insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000350721.9:c.810_811insT MANE Select ENSP00000343741.4:p.Ser271Ter
ENST00000515149.3:c.293-1171_293-1170insT ENSP00000425897.3:n.293-1171_293-1170insT
ENST00000653868.1:n.839_840insT
ENST00000657914.1:n.3168_3169insT
ENST00000659195.1:n.2875_2876insT
ENST00000661310.1:c.810_811insT ENSP00000499589.1:p.Ser271Ter
ENST00000350721.8:c.810_811insT ENSP00000343741.4:p.Ser271Ter
ENST00000507148.1:c.293-244_293-243insT ENSP00000426595.1:n.293-244_293-243insT
NM_001184.3:c.810_811insT NP_001175.2:p.Ser271Ter
XM_011512924.1:c.810_811insT XP_011511226.1:p.Ser271Ter
XM_011512925.1:c.810_811insT XP_011511227.1:p.Ser271Ter
XM_011512926.1:c.810_811insT XP_011511228.1:p.Ser271Ter
XM_011512927.1:c.810_811insT XP_011511229.1:p.Ser271Ter
XR_924147.1:n.899_900insT
XR_924148.1:n.899_900insT
XR_924149.1:n.899_900insT
NM_001354579.1:c.810_811insT NP_001341508.1:p.Ser271Ter
XR_001740179.2:n.899_900insT
XR_001740180.2:n.899_900insT
XR_001740181.2:n.899_900insT
XR_001740182.1:n.899_900insT
XR_002959543.1:n.899_900insT
XR_924148.2:n.899_900insT
NM_001184.4:c.810_811insT MANE Select NP_001175.2:p.Ser271Ter
NM_001354579.2:c.810_811insT NP_001341508.1:p.Ser271Ter