Canonical Allele Identifier: CA2577924885
Gene: ATR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142470251T>A , CM000665.2:g.142470251T>A GRCh38
NC_000003.11:g.142189093T>A , CM000665.1:g.142189093T>A GRCh37
NC_000003.10:g.143671783T>A NCBI36
NG_008951.1:g.113576A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000350721.9:c.6222-68A>T MANE Select ENSP00000343741.4:n.6222-68A>T
ENST00000513291.2:n.1406-68A>T
ENST00000654170.1:n.1065-68A>T
ENST00000656590.1:c.5012-68A>T
ENST00000661310.1:c.6030-68A>T ENSP00000499589.1:n.6030-68A>T
ENST00000665483.1:n.77-68A>T
ENST00000666447.1:n.57-68A>T
ENST00000666943.1:n.1686-68A>T
ENST00000350721.8:c.6222-68A>T ENSP00000343741.4:n.6222-68A>T
NM_001184.3:c.6222-68A>T NP_001175.2:n.6222-68A>T
XM_011512924.1:c.6228-68A>T XP_011511226.1:n.6228-68A>T
XM_011512925.1:c.6036-68A>T XP_011511227.1:n.6036-68A>T
XR_924147.1:n.6317-68A>T
XR_924148.1:n.6317-68A>T
XR_924149.1:n.6196-68A>T
NM_001354579.1:c.6030-68A>T NP_001341508.1:n.6030-68A>T
XR_001740179.2:n.6311-68A>T
XR_001740180.2:n.6365-68A>T
XR_001740181.2:n.6244-68A>T
XR_001740182.1:n.6196-68A>T
XR_002959543.1:n.6421-68A>T
XR_924148.2:n.6317-68A>T
NM_001184.4:c.6222-68A>T MANE Select NP_001175.2:n.6222-68A>T
NM_001354579.2:c.6030-68A>T NP_001341508.1:n.6030-68A>T