Canonical Allele Identifier: CA354814569

Gene: ATR

Linked Data

• ClinVar Variation Id: 1795229
• ClinVar RCV Id: RCV002431324
• MyVariant Identifiers: chr3:g.142272149T>C (hg19) ; chr3:g.142553307T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142553307T>C , CM000665.2:g.142553307T>C	GRCh38
NC_000003.11:g.142272149T>C , CM000665.1:g.142272149T>C	GRCh37
NC_000003.10:g.143754839T>C	NCBI36
NG_008951.1:g.30520A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.2725A>G MANE Select	ENSP00000343741.4:p.Thr909Ala
ENST00000515149.3:c.*1499A>G	ENSP00000425897.3:n.*1499A>G
ENST00000653868.1:n.2754A>G
ENST00000656590.1:c.1515A>G
ENST00000659195.1:n.5600A>G
ENST00000661310.1:c.2533A>G	ENSP00000499589.1:p.Thr845Ala
ENST00000350721.8:c.2725A>G	ENSP00000343741.4:p.Thr909Ala
NM_001184.3:c.2725A>G	NP_001175.2:p.Thr909Ala
XM_011512924.1:c.2725A>G	XP_011511226.1:p.Thr909Ala
XM_011512925.1:c.2533A>G	XP_011511227.1:p.Thr845Ala
XM_011512926.1:c.2725A>G	XP_011511228.1:p.Thr909Ala
XM_011512927.1:c.2725A>G	XP_011511229.1:p.Thr909Ala
XR_924147.1:n.2814A>G
XR_924148.1:n.2814A>G
XR_924149.1:n.2814A>G
NM_001354579.1:c.2533A>G	NP_001341508.1:p.Thr845Ala
XR_001740179.2:n.2814A>G
XR_001740180.2:n.2814A>G
XR_001740181.2:n.2814A>G
XR_001740182.1:n.2814A>G
XR_002959543.1:n.2814A>G
XR_924148.2:n.2814A>G
NM_001184.4:c.2725A>G MANE Select	NP_001175.2:p.Thr909Ala
NM_001354579.2:c.2533A>G	NP_001341508.1:p.Thr845Ala