Canonical Allele Identifier: CA354804341

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142188213T>G (hg19) ; chr3:g.142469371T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142469371T>G , CM000665.2:g.142469371T>G	GRCh38
NC_000003.11:g.142188213T>G , CM000665.1:g.142188213T>G	GRCh37
NC_000003.10:g.143670903T>G	NCBI36
NG_008951.1:g.114456A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6518A>C MANE Select	ENSP00000343741.4:p.Gln2173Pro
ENST00000513291.2:n.1702A>C
ENST00000654170.1:n.1361A>C
ENST00000656590.1:c.5308A>C
ENST00000661310.1:c.6326A>C	ENSP00000499589.1:p.Gln2109Pro
ENST00000665483.1:n.373A>C
ENST00000666447.1:n.353A>C
ENST00000666943.1:n.1982A>C
ENST00000350721.8:c.6518A>C	ENSP00000343741.4:p.Gln2173Pro
ENST00000513291.1:c.57A>C
NM_001184.3:c.6518A>C	NP_001175.2:p.Gln2173Pro
XM_011512924.1:c.6524A>C	XP_011511226.1:p.Gln2175Pro
XM_011512925.1:c.6332A>C	XP_011511227.1:p.Gln2111Pro
XR_924147.1:n.6613A>C
XR_924148.1:n.6613A>C
XR_924149.1:n.6492A>C
NM_001354579.1:c.6326A>C	NP_001341508.1:p.Gln2109Pro
XR_001740179.2:n.6607A>C
XR_924148.2:n.6613A>C
NM_001184.4:c.6518A>C MANE Select	NP_001175.2:p.Gln2173Pro
NM_001354579.2:c.6326A>C	NP_001341508.1:p.Gln2109Pro