Canonical Allele Identifier: CA354804428

Gene: ATR

Linked Data

• dbSNP Id: rs2108278762
• MyVariant Identifiers: chr3:g.142188227A>T (hg19) ; chr3:g.142469385A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142469385A>T , CM000665.2:g.142469385A>T	GRCh38
NC_000003.11:g.142188227A>T , CM000665.1:g.142188227A>T	GRCh37
NC_000003.10:g.143670917A>T	NCBI36
NG_008951.1:g.114442T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6504T>A MANE Select	ENSP00000343741.4:p.Phe2168Leu
ENST00000513291.2:n.1688T>A
ENST00000654170.1:n.1347T>A
ENST00000656590.1:c.5294T>A
ENST00000661310.1:c.6312T>A	ENSP00000499589.1:p.Phe2104Leu
ENST00000665483.1:n.359T>A
ENST00000666447.1:n.339T>A
ENST00000666943.1:n.1968T>A
ENST00000350721.8:c.6504T>A	ENSP00000343741.4:p.Phe2168Leu
ENST00000513291.1:c.43T>A
NM_001184.3:c.6504T>A	NP_001175.2:p.Phe2168Leu
XM_011512924.1:c.6510T>A	XP_011511226.1:p.Phe2170Leu
XM_011512925.1:c.6318T>A	XP_011511227.1:p.Phe2106Leu
XR_924147.1:n.6599T>A
XR_924148.1:n.6599T>A
XR_924149.1:n.6478T>A
NM_001354579.1:c.6312T>A	NP_001341508.1:p.Phe2104Leu
XR_001740179.2:n.6593T>A
XR_924148.2:n.6599T>A
NM_001184.4:c.6504T>A MANE Select	NP_001175.2:p.Phe2168Leu
NM_001354579.2:c.6312T>A	NP_001341508.1:p.Phe2104Leu