Canonical Allele Identifier: CA354793885

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142168395T>A (hg19) ; chr3:g.142449553T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142449553T>A , CM000665.2:g.142449553T>A	GRCh38
NC_000003.11:g.142168395T>A , CM000665.1:g.142168395T>A	GRCh37
NC_000003.10:g.143651085T>A	NCBI36
NG_008951.1:g.134274A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.7811A>T MANE Select	ENSP00000343741.4:p.Lys2604Met
ENST00000513291.2:n.6520A>T
ENST00000653893.1:n.2669A>T
ENST00000654170.1:n.2654A>T
ENST00000656114.1:n.2897A>T
ENST00000656590.1:c.6738A>T
ENST00000658083.1:n.2991A>T
ENST00000661310.1:c.7619A>T	ENSP00000499589.1:p.Lys2540Met
ENST00000665483.1:n.5351A>T
ENST00000666447.1:n.4314A>T
ENST00000666943.1:n.4543A>T
ENST00000350721.8:c.7811A>T	ENSP00000343741.4:p.Lys2604Met
ENST00000504521.5:c.400A>T	ENSP00000422553.1:n.400A>T
ENST00000513291.1:c.4875A>T
ENST00000515810.1:c.237A>T	ENSP00000421870.1:n.237A>T
NM_001184.3:c.7811A>T	NP_001175.2:p.Lys2604Met
XM_011512924.1:c.7817A>T	XP_011511226.1:p.Lys2606Met
XM_011512925.1:c.7625A>T	XP_011511227.1:p.Lys2542Met
XR_924147.1:n.10568A>T
XR_924148.1:n.8043A>T
NM_001354579.1:c.7619A>T	NP_001341508.1:p.Lys2540Met
XR_001740179.2:n.8037A>T
XR_924148.2:n.8043A>T
NM_001184.4:c.7811A>T MANE Select	NP_001175.2:p.Lys2604Met
NM_001354579.2:c.7619A>T	NP_001341508.1:p.Lys2540Met