Canonical Allele Identifier: CA2577925488

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142553429_142553432dup , CM000665.2:g.142553429_142553432dup	GRCh38
NC_000003.11:g.142272271_142272274dup , CM000665.1:g.142272271_142272274dup	GRCh37
NC_000003.10:g.143754961_143754964dup	NCBI36
NG_008951.1:g.30396_30399dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.2634-33_2634-30dup MANE Select	ENSP00000343741.4:n.2634-33_2634-30dup
ENST00000515149.3:c.*1408-33_*1408-30dup	ENSP00000425897.3:n.*1408-33_*1408-30dup
ENST00000653868.1:n.2663-33_2663-30dup
ENST00000656590.1:c.1424-33_1424-30dup
ENST00000659195.1:n.5509-33_5509-30dup
ENST00000661310.1:c.2442-33_2442-30dup	ENSP00000499589.1:n.2442-33_2442-30dup
ENST00000350721.8:c.2634-33_2634-30dup	ENSP00000343741.4:n.2634-33_2634-30dup
NM_001184.3:c.2634-33_2634-30dup	NP_001175.2:n.2634-33_2634-30dup
XM_011512924.1:c.2634-33_2634-30dup	XP_011511226.1:n.2634-33_2634-30dup
XM_011512925.1:c.2442-33_2442-30dup	XP_011511227.1:n.2442-33_2442-30dup
XM_011512926.1:c.2634-33_2634-30dup	XP_011511228.1:n.2634-33_2634-30dup
XM_011512927.1:c.2634-33_2634-30dup	XP_011511229.1:n.2634-33_2634-30dup
XR_924147.1:n.2723-33_2723-30dup
XR_924148.1:n.2723-33_2723-30dup
XR_924149.1:n.2723-33_2723-30dup
NM_001354579.1:c.2442-33_2442-30dup	NP_001341508.1:n.2442-33_2442-30dup
XR_001740179.2:n.2723-33_2723-30dup
XR_001740180.2:n.2723-33_2723-30dup
XR_001740181.2:n.2723-33_2723-30dup
XR_001740182.1:n.2723-33_2723-30dup
XR_002959543.1:n.2723-33_2723-30dup
XR_924148.2:n.2723-33_2723-30dup
NM_001184.4:c.2634-33_2634-30dup MANE Select	NP_001175.2:n.2634-33_2634-30dup
NM_001354579.2:c.2442-33_2442-30dup	NP_001341508.1:n.2442-33_2442-30dup