Canonical Allele Identifier: CA354805524
Gene: ATR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142470093C>T , CM000665.2:g.142470093C>T GRCh38
NC_000003.11:g.142188935C>T , CM000665.1:g.142188935C>T GRCh37
NC_000003.10:g.143671625C>T NCBI36
NG_008951.1:g.113734G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000350721.9:c.6312G>A MANE Select ENSP00000343741.4:p.Trp2104Ter
ENST00000513291.2:n.1496G>A
ENST00000654170.1:n.1155G>A
ENST00000656590.1:c.5102G>A
ENST00000661310.1:c.6120G>A ENSP00000499589.1:p.Trp2040Ter
ENST00000665483.1:n.167G>A
ENST00000666447.1:n.147G>A
ENST00000666943.1:n.1776G>A
ENST00000350721.8:c.6312G>A ENSP00000343741.4:p.Trp2104Ter
NM_001184.3:c.6312G>A NP_001175.2:p.Trp2104Ter
XM_011512924.1:c.6318G>A XP_011511226.1:p.Trp2106Ter
XM_011512925.1:c.6126G>A XP_011511227.1:p.Trp2042Ter
XR_924147.1:n.6407G>A
XR_924148.1:n.6407G>A
XR_924149.1:n.6286G>A
NM_001354579.1:c.6120G>A NP_001341508.1:p.Trp2040Ter
XR_001740179.2:n.6401G>A
XR_001740180.2:n.6455G>A
XR_001740181.2:n.6334G>A
XR_001740182.1:n.6286G>A
XR_002959543.1:n.6511G>A
XR_924148.2:n.6407G>A
NM_001184.4:c.6312G>A MANE Select NP_001175.2:p.Trp2104Ter
NM_001354579.2:c.6120G>A NP_001341508.1:p.Trp2040Ter