Canonical Allele Identifier: CA354804291

Gene: ATR

Linked Data

• dbSNP Id: rs2071204593
• MyVariant Identifiers: chr3:g.142188208C>T (hg19) ; chr3:g.142469366C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142469366C>T , CM000665.2:g.142469366C>T	GRCh38
NC_000003.11:g.142188208C>T , CM000665.1:g.142188208C>T	GRCh37
NC_000003.10:g.143670898C>T	NCBI36
NG_008951.1:g.114461G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6523G>A MANE Select	ENSP00000343741.4:p.Ala2175Thr
ENST00000513291.2:n.1707G>A
ENST00000654170.1:n.1366G>A
ENST00000656590.1:c.5313G>A
ENST00000661310.1:c.6331G>A	ENSP00000499589.1:p.Ala2111Thr
ENST00000665483.1:n.378G>A
ENST00000666447.1:n.358G>A
ENST00000666943.1:n.1987G>A
ENST00000350721.8:c.6523G>A	ENSP00000343741.4:p.Ala2175Thr
ENST00000513291.1:c.62G>A
NM_001184.3:c.6523G>A	NP_001175.2:p.Ala2175Thr
XM_011512924.1:c.6529G>A	XP_011511226.1:p.Ala2177Thr
XM_011512925.1:c.6337G>A	XP_011511227.1:p.Ala2113Thr
XR_924147.1:n.6618G>A
XR_924148.1:n.6618G>A
XR_924149.1:n.6497G>A
NM_001354579.1:c.6331G>A	NP_001341508.1:p.Ala2111Thr
XR_001740179.2:n.6612G>A
XR_924148.2:n.6618G>A
NM_001184.4:c.6523G>A MANE Select	NP_001175.2:p.Ala2175Thr
NM_001354579.2:c.6331G>A	NP_001341508.1:p.Ala2111Thr