Canonical Allele Identifier: CA354793930

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142168416T>C (hg19) ; chr3:g.142449574T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142449574T>C , CM000665.2:g.142449574T>C	GRCh38
NC_000003.11:g.142168416T>C , CM000665.1:g.142168416T>C	GRCh37
NC_000003.10:g.143651106T>C	NCBI36
NG_008951.1:g.134253A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.7790A>G MANE Select	ENSP00000343741.4:p.Gln2597Arg
ENST00000513291.2:n.6499A>G
ENST00000653893.1:n.2648A>G
ENST00000654170.1:n.2633A>G
ENST00000656114.1:n.2876A>G
ENST00000656590.1:c.6717A>G
ENST00000658083.1:n.2970A>G
ENST00000661310.1:c.7598A>G	ENSP00000499589.1:p.Gln2533Arg
ENST00000665483.1:n.5330A>G
ENST00000666447.1:n.4293A>G
ENST00000666943.1:n.4522A>G
ENST00000350721.8:c.7790A>G	ENSP00000343741.4:p.Gln2597Arg
ENST00000504521.5:c.379A>G	ENSP00000422553.1:n.379A>G
ENST00000513291.1:c.4854A>G
ENST00000515810.1:c.216A>G	ENSP00000421870.1:n.216A>G
NM_001184.3:c.7790A>G	NP_001175.2:p.Gln2597Arg
XM_011512924.1:c.7796A>G	XP_011511226.1:p.Gln2599Arg
XM_011512925.1:c.7604A>G	XP_011511227.1:p.Gln2535Arg
XR_924147.1:n.10547A>G
XR_924148.1:n.8022A>G
NM_001354579.1:c.7598A>G	NP_001341508.1:p.Gln2533Arg
XR_001740179.2:n.8016A>G
XR_924148.2:n.8022A>G
NM_001184.4:c.7790A>G MANE Select	NP_001175.2:p.Gln2597Arg
NM_001354579.2:c.7598A>G	NP_001341508.1:p.Gln2533Arg