Canonical Allele Identifier: CA1407031582
Gene: ATR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142562391A= , CM000665.2:g.142562391A= GRCh38
NC_000003.11:g.142281233A= , CM000665.1:g.142281233A= GRCh37
NC_000003.10:g.143763923A= NCBI36
NG_008951.1:g.21436T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000350721.9:c.1011T= MANE Select ENSP00000343741.4:p.Leu337=
ENST00000515149.3:c.293-970T= ENSP00000425897.3:n.293-970T=
ENST00000653868.1:n.1040T=
ENST00000657914.1:n.3369T=
ENST00000659195.1:n.3076T=
ENST00000661310.1:c.1011T= ENSP00000499589.1:p.Leu337=
ENST00000350721.8:c.1011T= ENSP00000343741.4:p.Leu337=
ENST00000507148.1:c.293-43T= ENSP00000426595.1:n.293-43T=
ENST00000515149.2:c.54T= ENSP00000425897.2:p.Leu18=
NM_001184.3:c.1011T= NP_001175.2:p.Leu337=
XM_011512924.1:c.1011T= XP_011511226.1:p.Leu337=
XM_011512925.1:c.1011T= XP_011511227.1:p.Leu337=
XM_011512926.1:c.1011T= XP_011511228.1:p.Leu337=
XM_011512927.1:c.1011T= XP_011511229.1:p.Leu337=
XR_924147.1:n.1100T=
XR_924148.1:n.1100T=
XR_924149.1:n.1100T=
NM_001354579.1:c.1011T= NP_001341508.1:p.Leu337=
XR_001740179.2:n.1100T=
XR_001740180.2:n.1100T=
XR_001740181.2:n.1100T=
XR_001740182.1:n.1100T=
XR_002959543.1:n.1100T=
XR_924148.2:n.1100T=
NM_001184.4:c.1011T= MANE Select NP_001175.2:p.Leu337=
NM_001354579.2:c.1011T= NP_001341508.1:p.Leu337=