Canonical Allele Identifier: CA2668041681

Gene: ATR

Linked Data

• gnomAD v4: 3-142513459-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142513459A>C , CM000665.2:g.142513459A>C	GRCh38
NC_000003.11:g.142232301A>C , CM000665.1:g.142232301A>C	GRCh37
NC_000003.10:g.143714991A>C	NCBI36
NG_008951.1:g.70368T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.4641+42T>G MANE Select	ENSP00000343741.4:n.4641+42T>G
ENST00000653868.1:n.4670+42T>G
ENST00000656590.1:c.3431+42T>G
ENST00000661310.1:c.4449+42T>G	ENSP00000499589.1:n.4449+42T>G
ENST00000666943.1:n.105+42T>G
ENST00000350721.8:c.4641+42T>G	ENSP00000343741.4:n.4641+42T>G
NM_001184.3:c.4641+42T>G	NP_001175.2:n.4641+42T>G
XM_011512924.1:c.4647+42T>G	XP_011511226.1:n.4647+42T>G
XM_011512925.1:c.4455+42T>G	XP_011511227.1:n.4455+42T>G
XM_011512926.1:c.4647+42T>G	XP_011511228.1:n.4647+42T>G
XM_011512927.1:c.4647+42T>G	XP_011511229.1:n.4647+42T>G
XR_924147.1:n.4736+42T>G
XR_924148.1:n.4736+42T>G
XR_924149.1:n.4736+42T>G
NM_001354579.1:c.4449+42T>G	NP_001341508.1:n.4449+42T>G
XR_001740179.2:n.4730+42T>G
XR_001740180.2:n.4736+42T>G
XR_001740181.2:n.4736+42T>G
XR_001740182.1:n.4736+42T>G
XR_002959543.1:n.4736+42T>G
XR_924148.2:n.4736+42T>G
NM_001184.4:c.4641+42T>G MANE Select	NP_001175.2:n.4641+42T>G
NM_001354579.2:c.4449+42T>G	NP_001341508.1:n.4449+42T>G