Canonical Allele Identifier: CA354805539

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142188939T>A (hg19) ; chr3:g.142470097T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470097T>A , CM000665.2:g.142470097T>A	GRCh38
NC_000003.11:g.142188939T>A , CM000665.1:g.142188939T>A	GRCh37
NC_000003.10:g.143671629T>A	NCBI36
NG_008951.1:g.113730A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000350721.9:c.6308A>T MANE Select	ENSP00000343741.4:p.Glu2103Val
ENST00000513291.2:n.1492A>T
ENST00000654170.1:n.1151A>T
ENST00000656590.1:c.5098A>T
ENST00000661310.1:c.6116A>T	ENSP00000499589.1:p.Glu2039Val
ENST00000665483.1:n.163A>T
ENST00000666447.1:n.143A>T
ENST00000666943.1:n.1772A>T
ENST00000350721.8:c.6308A>T	ENSP00000343741.4:p.Glu2103Val
NM_001184.3:c.6308A>T	NP_001175.2:p.Glu2103Val
XM_011512924.1:c.6314A>T	XP_011511226.1:p.Glu2105Val
XM_011512925.1:c.6122A>T	XP_011511227.1:p.Glu2041Val
XR_924147.1:n.6403A>T
XR_924148.1:n.6403A>T
XR_924149.1:n.6282A>T
NM_001354579.1:c.6116A>T	NP_001341508.1:p.Glu2039Val
XR_001740179.2:n.6397A>T
XR_001740180.2:n.6451A>T
XR_001740181.2:n.6330A>T
XR_001740182.1:n.6282A>T
XR_002959543.1:n.6507A>T
XR_924148.2:n.6403A>T
NM_001184.4:c.6308A>T MANE Select	NP_001175.2:p.Glu2103Val
NM_001354579.2:c.6116A>T	NP_001341508.1:p.Glu2039Val