Canonical Allele Identifier: CA84721306

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142452849A>T , CM000665.2:g.142452849A>T	GRCh38
NC_000003.11:g.142171691A>T , CM000665.1:g.142171691A>T	GRCh37
NC_000003.10:g.143654381A>T	NCBI36
NG_008951.1:g.130978T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001184.4:c.7761+279T>A MANE Select	NP_001175.2:n.7761+279T>A
ENST00000350721.9:c.7761+279T>A MANE Select	ENSP00000343741.4:n.7761+279T>A
NM_001184.3:c.7761+279T>A	NP_001175.2:n.7761+279T>A
NM_001354579.1:c.7569+279T>A	NP_001341508.1:n.7569+279T>A
NM_001354579.2:c.7569+279T>A	NP_001341508.1:n.7569+279T>A
ENST00000350721.8:c.7761+279T>A	ENSP00000343741.4:n.7761+279T>A
ENST00000504521.5:c.213+279T>A	ENSP00000422553.1:n.213+279T>A
ENST00000511016.1:n.585T>A
ENST00000513291.1:c.1579T>A
ENST00000513291.2:n.3224T>A
ENST00000515810.1:c.50+268T>A	ENSP00000421870.1:n.50+268T>A
ENST00000653893.1:n.2619+279T>A
ENST00000654170.1:n.2604+279T>A
ENST00000656114.1:n.2847+279T>A
ENST00000656590.1:c.6551+279T>A
ENST00000658083.1:n.2804+279T>A
ENST00000661310.1:c.7569+279T>A	ENSP00000499589.1:n.7569+279T>A
ENST00000665483.1:n.5301+279T>A
ENST00000666447.1:n.4264+279T>A
ENST00000666943.1:n.4493+279T>A
XM_011512924.1:c.7767+279T>A	XP_011511226.1:n.7767+279T>A
XM_011512925.1:c.7575+279T>A	XP_011511227.1:n.7575+279T>A
XR_001740179.2:n.7850+279T>A
XR_924147.1:n.8135T>A
XR_924148.1:n.7856+279T>A
XR_924148.2:n.7856+279T>A