Canonical Allele Identifier: CA354807473
Community Standard Title: NM_001184.4(ATR):c.3674T>A (p.Ile1225Asn)
Gene: ATR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142538533A>T , CM000665.2:g.142538533A>T GRCh38
NC_000003.11:g.142257375A>T , CM000665.1:g.142257375A>T GRCh37
NC_000003.10:g.143740065A>T NCBI36
NG_008951.1:g.45294T>A

Transcript Alleles

HGVS Amino-acid Change
NM_001184.4:c.3674T>A MANE Select NP_001175.2:p.Ile1225Asn
ENST00000350721.9:c.3674T>A MANE Select ENSP00000343741.4:p.Ile1225Asn
NM_001184.3:c.3674T>A NP_001175.2:p.Ile1225Asn
NM_001354579.1:c.3482T>A NP_001341508.1:p.Ile1161Asn
NM_001354579.2:c.3482T>A NP_001341508.1:p.Ile1161Asn
ENST00000350721.8:c.3674T>A ENSP00000343741.4:p.Ile1225Asn
ENST00000515149.3:c.*2448T>A ENSP00000425897.3:n.*2448T>A
ENST00000653868.1:n.3703T>A
ENST00000656582.1:n.933T>A
ENST00000656590.1:c.2464T>A
ENST00000661310.1:c.3482T>A ENSP00000499589.1:p.Ile1161Asn
XM_011512924.1:c.3674T>A XP_011511226.1:p.Ile1225Asn
XM_011512925.1:c.3482T>A XP_011511227.1:p.Ile1161Asn
XM_011512926.1:c.3674T>A XP_011511228.1:p.Ile1225Asn
XM_011512927.1:c.3674T>A XP_011511229.1:p.Ile1225Asn
XR_001740179.2:n.3763T>A
XR_001740180.2:n.3763T>A
XR_001740181.2:n.3763T>A
XR_001740182.1:n.3763T>A
XR_002959543.1:n.3763T>A
XR_924147.1:n.3763T>A
XR_924148.1:n.3763T>A
XR_924148.2:n.3763T>A
XR_924149.1:n.3763T>A