Canonical Allele Identifier: CA354793896

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142168401A>T (hg19) ; chr3:g.142449559A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142449559A>T , CM000665.2:g.142449559A>T	GRCh38
NC_000003.11:g.142168401A>T , CM000665.1:g.142168401A>T	GRCh37
NC_000003.10:g.143651091A>T	NCBI36
NG_008951.1:g.134268T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000350721.9:c.7805T>A MANE Select	ENSP00000343741.4:p.Val2602Glu
ENST00000513291.2:n.6514T>A
ENST00000653893.1:n.2663T>A
ENST00000654170.1:n.2648T>A
ENST00000656114.1:n.2891T>A
ENST00000656590.1:c.6732T>A
ENST00000658083.1:n.2985T>A
ENST00000661310.1:c.7613T>A	ENSP00000499589.1:p.Val2538Glu
ENST00000665483.1:n.5345T>A
ENST00000666447.1:n.4308T>A
ENST00000666943.1:n.4537T>A
ENST00000350721.8:c.7805T>A	ENSP00000343741.4:p.Val2602Glu
ENST00000504521.5:c.394T>A	ENSP00000422553.1:n.394T>A
ENST00000513291.1:c.4869T>A
ENST00000515810.1:c.231T>A	ENSP00000421870.1:n.231T>A
NM_001184.3:c.7805T>A	NP_001175.2:p.Val2602Glu
XM_011512924.1:c.7811T>A	XP_011511226.1:p.Val2604Glu
XM_011512925.1:c.7619T>A	XP_011511227.1:p.Val2540Glu
XR_924147.1:n.10562T>A
XR_924148.1:n.8037T>A
NM_001354579.1:c.7613T>A	NP_001341508.1:p.Val2538Glu
XR_001740179.2:n.8031T>A
XR_924148.2:n.8037T>A
NM_001184.4:c.7805T>A MANE Select	NP_001175.2:p.Val2602Glu
NM_001354579.2:c.7613T>A	NP_001341508.1:p.Val2538Glu