Canonical Allele Identifier: CA354805890

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142188991A>T (hg19) ; chr3:g.142470149A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470149A>T , CM000665.2:g.142470149A>T	GRCh38
NC_000003.11:g.142188991A>T , CM000665.1:g.142188991A>T	GRCh37
NC_000003.10:g.143671681A>T	NCBI36
NG_008951.1:g.113678T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6256T>A MANE Select	ENSP00000343741.4:p.Ser2086Thr
ENST00000513291.2:n.1440T>A
ENST00000654170.1:n.1099T>A
ENST00000656590.1:c.5046T>A
ENST00000661310.1:c.6064T>A	ENSP00000499589.1:p.Ser2022Thr
ENST00000665483.1:n.111T>A
ENST00000666447.1:n.91T>A
ENST00000666943.1:n.1720T>A
ENST00000350721.8:c.6256T>A	ENSP00000343741.4:p.Ser2086Thr
NM_001184.3:c.6256T>A	NP_001175.2:p.Ser2086Thr
XM_011512924.1:c.6262T>A	XP_011511226.1:p.Ser2088Thr
XM_011512925.1:c.6070T>A	XP_011511227.1:p.Ser2024Thr
XR_924147.1:n.6351T>A
XR_924148.1:n.6351T>A
XR_924149.1:n.6230T>A
NM_001354579.1:c.6064T>A	NP_001341508.1:p.Ser2022Thr
XR_001740179.2:n.6345T>A
XR_001740180.2:n.6399T>A
XR_001740181.2:n.6278T>A
XR_001740182.1:n.6230T>A
XR_002959543.1:n.6455T>A
XR_924148.2:n.6351T>A
NM_001184.4:c.6256T>A MANE Select	NP_001175.2:p.Ser2086Thr
NM_001354579.2:c.6064T>A	NP_001341508.1:p.Ser2022Thr