Canonical Allele Identifier: CA1406992031
Gene: ATR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142470502_142470503delinsCA , CM000665.2:g.142470502_142470503delinsCA GRCh38
NC_000003.11:g.142189344_142189345delinsCA , CM000665.1:g.142189344_142189345delinsCA GRCh37
NC_000003.10:g.143672034_143672035delinsCA NCBI36
NG_008951.1:g.113324_113325delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000350721.9:c.6222-320_6222-319delinsTG MANE Select ENSP00000343741.4:n.6222-320_6222-319delinsTG
ENST00000513291.2:n.1406-320_1406-319delinsTG
ENST00000654170.1:n.1065-320_1065-319delinsTG
ENST00000656590.1:c.5012-320_5012-319delinsTG
ENST00000661310.1:c.6030-320_6030-319delinsTG ENSP00000499589.1:n.6030-320_6030-319delinsTG
ENST00000665483.1:n.77-320_77-319delinsTG
ENST00000666447.1:n.57-320_57-319delinsTG
ENST00000666943.1:n.1686-320_1686-319delinsTG
ENST00000350721.8:c.6222-320_6222-319delinsTG ENSP00000343741.4:n.6222-320_6222-319delinsTG
NM_001184.3:c.6222-320_6222-319delinsTG NP_001175.2:n.6222-320_6222-319delinsTG
XM_011512924.1:c.6228-320_6228-319delinsTG XP_011511226.1:n.6228-320_6228-319delinsTG
XM_011512925.1:c.6036-320_6036-319delinsTG XP_011511227.1:n.6036-320_6036-319delinsTG
XR_924147.1:n.6317-320_6317-319delinsTG
XR_924148.1:n.6317-320_6317-319delinsTG
XR_924149.1:n.6196-320_6196-319delinsTG
NM_001354579.1:c.6030-320_6030-319delinsTG NP_001341508.1:n.6030-320_6030-319delinsTG
XR_001740179.2:n.6311-320_6311-319delinsTG
XR_001740180.2:n.6365-320_6365-319delinsTG
XR_001740181.2:n.6244-320_6244-319delinsTG
XR_001740182.1:n.6196-320_6196-319delinsTG
XR_002959543.1:n.6421-320_6421-319delinsTG
XR_924148.2:n.6317-320_6317-319delinsTG
NM_001184.4:c.6222-320_6222-319delinsTG MANE Select NP_001175.2:n.6222-320_6222-319delinsTG
NM_001354579.2:c.6030-320_6030-319delinsTG NP_001341508.1:n.6030-320_6030-319delinsTG