Canonical Allele Identifier: CA1054330672

Gene: ATR

Linked Data

• dbSNP Id: rs2032719362
• gnomAD v3: 3-142513862-T-G
• gnomAD v4: 3-142513862-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142513862T>G , CM000665.2:g.142513862T>G	GRCh38
NC_000003.11:g.142232704T>G , CM000665.1:g.142232704T>G	GRCh37
NC_000003.10:g.143715394T>G	NCBI36
NG_008951.1:g.69965A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.4504-224A>C MANE Select	ENSP00000343741.4:n.4504-224A>C
ENST00000653868.1:n.4533-224A>C
ENST00000656590.1:c.3294-224A>C
ENST00000661310.1:c.4312-224A>C	ENSP00000499589.1:n.4312-224A>C
ENST00000350721.8:c.4504-224A>C	ENSP00000343741.4:n.4504-224A>C
NM_001184.3:c.4504-224A>C	NP_001175.2:n.4504-224A>C
XM_011512924.1:c.4510-224A>C	XP_011511226.1:n.4510-224A>C
XM_011512925.1:c.4318-224A>C	XP_011511227.1:n.4318-224A>C
XM_011512926.1:c.4510-224A>C	XP_011511228.1:n.4510-224A>C
XM_011512927.1:c.4510-224A>C	XP_011511229.1:n.4510-224A>C
XR_924147.1:n.4599-224A>C
XR_924148.1:n.4599-224A>C
XR_924149.1:n.4599-224A>C
NM_001354579.1:c.4312-224A>C	NP_001341508.1:n.4312-224A>C
XR_001740179.2:n.4593-224A>C
XR_001740180.2:n.4599-224A>C
XR_001740181.2:n.4599-224A>C
XR_001740182.1:n.4599-224A>C
XR_002959543.1:n.4599-224A>C
XR_924148.2:n.4599-224A>C
NM_001184.4:c.4504-224A>C MANE Select	NP_001175.2:n.4504-224A>C
NM_001354579.2:c.4312-224A>C	NP_001341508.1:n.4312-224A>C