Canonical Allele Identifier: CA2668041667

Gene: ATR

Linked Data

• gnomAD v4: 3-142513428-C-CTT

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142513430_142513431dup , CM000665.2:g.142513430_142513431dup	GRCh38
NC_000003.11:g.142232272_142232273dup , CM000665.1:g.142232272_142232273dup	GRCh37
NC_000003.10:g.143714962_143714963dup	NCBI36
NG_008951.1:g.70397_70398dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.4641+71_4641+72dup MANE Select	ENSP00000343741.4:n.4641+71_4641+72dup
ENST00000653868.1:n.4670+71_4670+72dup
ENST00000656590.1:c.3431+71_3431+72dup
ENST00000661310.1:c.4449+71_4449+72dup	ENSP00000499589.1:n.4449+71_4449+72dup
ENST00000666943.1:n.105+71_105+72dup
ENST00000350721.8:c.4641+71_4641+72dup	ENSP00000343741.4:n.4641+71_4641+72dup
NM_001184.3:c.4641+71_4641+72dup	NP_001175.2:n.4641+71_4641+72dup
XM_011512924.1:c.4647+71_4647+72dup	XP_011511226.1:n.4647+71_4647+72dup
XM_011512925.1:c.4455+71_4455+72dup	XP_011511227.1:n.4455+71_4455+72dup
XM_011512926.1:c.4647+71_4647+72dup	XP_011511228.1:n.4647+71_4647+72dup
XM_011512927.1:c.4647+71_4647+72dup	XP_011511229.1:n.4647+71_4647+72dup
XR_924147.1:n.4736+71_4736+72dup
XR_924148.1:n.4736+71_4736+72dup
XR_924149.1:n.4736+71_4736+72dup
NM_001354579.1:c.4449+71_4449+72dup	NP_001341508.1:n.4449+71_4449+72dup
XR_001740179.2:n.4730+71_4730+72dup
XR_001740180.2:n.4736+71_4736+72dup
XR_001740181.2:n.4736+71_4736+72dup
XR_001740182.1:n.4736+71_4736+72dup
XR_002959543.1:n.4736+71_4736+72dup
XR_924148.2:n.4736+71_4736+72dup
NM_001184.4:c.4641+71_4641+72dup MANE Select	NP_001175.2:n.4641+71_4641+72dup
NM_001354579.2:c.4449+71_4449+72dup	NP_001341508.1:n.4449+71_4449+72dup