Canonical Allele Identifier: CA2668036940

Gene: ATR

Linked Data

• gnomAD v4: 3-142449616-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142449616A>T , CM000665.2:g.142449616A>T	GRCh38
NC_000003.11:g.142168458A>T , CM000665.1:g.142168458A>T	GRCh37
NC_000003.10:g.143651148A>T	NCBI36
NG_008951.1:g.134211T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.7762-14T>A MANE Select	ENSP00000343741.4:n.7762-14T>A
ENST00000513291.2:n.6457T>A
ENST00000653893.1:n.2620-14T>A
ENST00000654170.1:n.2605-14T>A
ENST00000656114.1:n.2848-14T>A
ENST00000656590.1:c.6689-14T>A
ENST00000658083.1:n.2942-14T>A
ENST00000661310.1:c.7570-14T>A	ENSP00000499589.1:n.7570-14T>A
ENST00000665483.1:n.5302-14T>A
ENST00000666447.1:n.4265-14T>A
ENST00000666943.1:n.4494-14T>A
ENST00000350721.8:c.7762-14T>A	ENSP00000343741.4:n.7762-14T>A
ENST00000504521.5:c.351-14T>A	ENSP00000422553.1:n.351-14T>A
ENST00000513291.1:c.4812T>A
ENST00000515810.1:c.188-14T>A	ENSP00000421870.1:n.188-14T>A
NM_001184.3:c.7762-14T>A	NP_001175.2:n.7762-14T>A
XM_011512924.1:c.7768-14T>A	XP_011511226.1:n.7768-14T>A
XM_011512925.1:c.7576-14T>A	XP_011511227.1:n.7576-14T>A
XR_924147.1:n.10519-14T>A
XR_924148.1:n.7994-14T>A
NM_001354579.1:c.7570-14T>A	NP_001341508.1:n.7570-14T>A
XR_001740179.2:n.7988-14T>A
XR_924148.2:n.7994-14T>A
NM_001184.4:c.7762-14T>A MANE Select	NP_001175.2:n.7762-14T>A
NM_001354579.2:c.7570-14T>A	NP_001341508.1:n.7570-14T>A