Canonical Allele Identifier: CA1406991550
Gene: ATR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142469289A= , CM000665.2:g.142469289A= GRCh38
NC_000003.11:g.142188131A= , CM000665.1:g.142188131A= GRCh37
NC_000003.10:g.143670821A= NCBI36
NG_008951.1:g.114538T=

Transcript Alleles

HGVS Amino-acid change
ENST00000350721.9:c.6552+48T= MANE Select ENSP00000343741.4:n.6552+48T=
ENST00000513291.2:n.1736+48T=
ENST00000654170.1:n.1395+48T=
ENST00000656590.1:c.5342+48T=
ENST00000661310.1:c.6360+48T= ENSP00000499589.1:n.6360+48T=
ENST00000665483.1:n.407+48T=
ENST00000666447.1:n.435T=
ENST00000666943.1:n.2064T=
ENST00000350721.8:c.6552+48T= ENSP00000343741.4:n.6552+48T=
ENST00000513291.1:c.91+48T=
NM_001184.3:c.6552+48T= NP_001175.2:n.6552+48T=
XM_011512924.1:c.6558+48T= XP_011511226.1:n.6558+48T=
XM_011512925.1:c.6366+48T= XP_011511227.1:n.6366+48T=
XR_924147.1:n.6647+48T=
XR_924148.1:n.6647+48T=
XR_924149.1:n.6526+48T=
NM_001354579.1:c.6360+48T= NP_001341508.1:n.6360+48T=
XR_001740179.2:n.6641+48T=
XR_924148.2:n.6647+48T=
NM_001184.4:c.6552+48T= MANE Select NP_001175.2:n.6552+48T=
NM_001354579.2:c.6360+48T= NP_001341508.1:n.6360+48T=