Canonical Allele Identifier: CA354796905

Gene: ATR

Linked Data

• ClinVar Variation Id: 1741640
• ClinVar RCV Id: RCV002342207
• MyVariant Identifiers: chr3:g.142232404T>G (hg19) ; chr3:g.142513562T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142513562T>G , CM000665.2:g.142513562T>G	GRCh38
NC_000003.11:g.142232404T>G , CM000665.1:g.142232404T>G	GRCh37
NC_000003.10:g.143715094T>G	NCBI36
NG_008951.1:g.70265A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.4580A>C MANE Select	ENSP00000343741.4:p.Tyr1527Ser
ENST00000653868.1:n.4609A>C
ENST00000656590.1:c.3370A>C
ENST00000661310.1:c.4388A>C	ENSP00000499589.1:p.Tyr1463Ser
ENST00000666943.1:n.44A>C
ENST00000350721.8:c.4580A>C	ENSP00000343741.4:p.Tyr1527Ser
NM_001184.3:c.4580A>C	NP_001175.2:p.Tyr1527Ser
XM_011512924.1:c.4586A>C	XP_011511226.1:p.Tyr1529Ser
XM_011512925.1:c.4394A>C	XP_011511227.1:p.Tyr1465Ser
XM_011512926.1:c.4586A>C	XP_011511228.1:p.Tyr1529Ser
XM_011512927.1:c.4586A>C	XP_011511229.1:p.Tyr1529Ser
XR_924147.1:n.4675A>C
XR_924148.1:n.4675A>C
XR_924149.1:n.4675A>C
NM_001354579.1:c.4388A>C	NP_001341508.1:p.Tyr1463Ser
XR_001740179.2:n.4669A>C
XR_001740180.2:n.4675A>C
XR_001740181.2:n.4675A>C
XR_001740182.1:n.4675A>C
XR_002959543.1:n.4675A>C
XR_924148.2:n.4675A>C
NM_001184.4:c.4580A>C MANE Select	NP_001175.2:p.Tyr1527Ser
NM_001354579.2:c.4388A>C	NP_001341508.1:p.Tyr1463Ser