Canonical Allele Identifier: CA1406991867
Gene: ATR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142470094C= , CM000665.2:g.142470094C= GRCh38
NC_000003.11:g.142188936C= , CM000665.1:g.142188936C= GRCh37
NC_000003.10:g.143671626C= NCBI36
NG_008951.1:g.113733G=

Transcript Alleles

HGVS Amino-acid change
ENST00000350721.9:c.6311G= MANE Select ENSP00000343741.4:p.Trp2104=
ENST00000513291.2:n.1495G=
ENST00000654170.1:n.1154G=
ENST00000656590.1:c.5101G=
ENST00000661310.1:c.6119G= ENSP00000499589.1:p.Trp2040=
ENST00000665483.1:n.166G=
ENST00000666447.1:n.146G=
ENST00000666943.1:n.1775G=
ENST00000350721.8:c.6311G= ENSP00000343741.4:p.Trp2104=
NM_001184.3:c.6311G= NP_001175.2:p.Trp2104=
XM_011512924.1:c.6317G= XP_011511226.1:p.Trp2106=
XM_011512925.1:c.6125G= XP_011511227.1:p.Trp2042=
XR_924147.1:n.6406G=
XR_924148.1:n.6406G=
XR_924149.1:n.6285G=
NM_001354579.1:c.6119G= NP_001341508.1:p.Trp2040=
XR_001740179.2:n.6400G=
XR_001740180.2:n.6454G=
XR_001740181.2:n.6333G=
XR_001740182.1:n.6285G=
XR_002959543.1:n.6510G=
XR_924148.2:n.6406G=
NM_001184.4:c.6311G= MANE Select NP_001175.2:p.Trp2104=
NM_001354579.2:c.6119G= NP_001341508.1:p.Trp2040=