Canonical Allele Identifier: CA1406991555
Gene: ATR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142469297A= , CM000665.2:g.142469297A= GRCh38
NC_000003.11:g.142188139A= , CM000665.1:g.142188139A= GRCh37
NC_000003.10:g.143670829A= NCBI36
NG_008951.1:g.114530T=

Transcript Alleles

HGVS Amino-acid change
ENST00000350721.9:c.6552+40T= MANE Select ENSP00000343741.4:n.6552+40T=
ENST00000513291.2:n.1736+40T=
ENST00000654170.1:n.1395+40T=
ENST00000656590.1:c.5342+40T=
ENST00000661310.1:c.6360+40T= ENSP00000499589.1:n.6360+40T=
ENST00000665483.1:n.407+40T=
ENST00000666447.1:n.427T=
ENST00000666943.1:n.2056T=
ENST00000350721.8:c.6552+40T= ENSP00000343741.4:n.6552+40T=
ENST00000513291.1:c.91+40T=
NM_001184.3:c.6552+40T= NP_001175.2:n.6552+40T=
XM_011512924.1:c.6558+40T= XP_011511226.1:n.6558+40T=
XM_011512925.1:c.6366+40T= XP_011511227.1:n.6366+40T=
XR_924147.1:n.6647+40T=
XR_924148.1:n.6647+40T=
XR_924149.1:n.6526+40T=
NM_001354579.1:c.6360+40T= NP_001341508.1:n.6360+40T=
XR_001740179.2:n.6641+40T=
XR_924148.2:n.6647+40T=
NM_001184.4:c.6552+40T= MANE Select NP_001175.2:n.6552+40T=
NM_001354579.2:c.6360+40T= NP_001341508.1:n.6360+40T=