Canonical Allele Identifier: CA2577924570

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142449636G>T , CM000665.2:g.142449636G>T	GRCh38
NC_000003.11:g.142168478G>T , CM000665.1:g.142168478G>T	GRCh37
NC_000003.10:g.143651168G>T	NCBI36
NG_008951.1:g.134191C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.7762-34C>A MANE Select	ENSP00000343741.4:n.7762-34C>A
ENST00000513291.2:n.6437C>A
ENST00000653893.1:n.2620-34C>A
ENST00000654170.1:n.2605-34C>A
ENST00000656114.1:n.2848-34C>A
ENST00000656590.1:c.6689-34C>A
ENST00000658083.1:n.2942-34C>A
ENST00000661310.1:c.7570-34C>A	ENSP00000499589.1:n.7570-34C>A
ENST00000665483.1:n.5302-34C>A
ENST00000666447.1:n.4265-34C>A
ENST00000666943.1:n.4494-34C>A
ENST00000350721.8:c.7762-34C>A	ENSP00000343741.4:n.7762-34C>A
ENST00000504521.5:c.351-34C>A	ENSP00000422553.1:n.351-34C>A
ENST00000513291.1:c.4792C>A
ENST00000515810.1:c.188-34C>A	ENSP00000421870.1:n.188-34C>A
NM_001184.3:c.7762-34C>A	NP_001175.2:n.7762-34C>A
XM_011512924.1:c.7768-34C>A	XP_011511226.1:n.7768-34C>A
XM_011512925.1:c.7576-34C>A	XP_011511227.1:n.7576-34C>A
XR_924147.1:n.10519-34C>A
XR_924148.1:n.7994-34C>A
NM_001354579.1:c.7570-34C>A	NP_001341508.1:n.7570-34C>A
XR_001740179.2:n.7988-34C>A
XR_924148.2:n.7994-34C>A
NM_001184.4:c.7762-34C>A MANE Select	NP_001175.2:n.7762-34C>A
NM_001354579.2:c.7570-34C>A	NP_001341508.1:n.7570-34C>A