Canonical Allele Identifier: CA354805509

Gene: ATR

Linked Data

• gnomAD v4: 3-142470091-T-C
• MyVariant Identifiers: chr3:g.142188933T>C (hg19) ; chr3:g.142470091T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470091T>C , CM000665.2:g.142470091T>C	GRCh38
NC_000003.11:g.142188933T>C , CM000665.1:g.142188933T>C	GRCh37
NC_000003.10:g.143671623T>C	NCBI36
NG_008951.1:g.113736A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000350721.9:c.6314A>G MANE Select	ENSP00000343741.4:p.Glu2105Gly
ENST00000513291.2:n.1498A>G
ENST00000654170.1:n.1157A>G
ENST00000656590.1:c.5104A>G
ENST00000661310.1:c.6122A>G	ENSP00000499589.1:p.Glu2041Gly
ENST00000665483.1:n.169A>G
ENST00000666447.1:n.149A>G
ENST00000666943.1:n.1778A>G
ENST00000350721.8:c.6314A>G	ENSP00000343741.4:p.Glu2105Gly
NM_001184.3:c.6314A>G	NP_001175.2:p.Glu2105Gly
XM_011512924.1:c.6320A>G	XP_011511226.1:p.Glu2107Gly
XM_011512925.1:c.6128A>G	XP_011511227.1:p.Glu2043Gly
XR_924147.1:n.6409A>G
XR_924148.1:n.6409A>G
XR_924149.1:n.6288A>G
NM_001354579.1:c.6122A>G	NP_001341508.1:p.Glu2041Gly
XR_001740179.2:n.6403A>G
XR_001740180.2:n.6457A>G
XR_001740181.2:n.6336A>G
XR_001740182.1:n.6288A>G
XR_002959543.1:n.6513A>G
XR_924148.2:n.6409A>G
NM_001184.4:c.6314A>G MANE Select	NP_001175.2:p.Glu2105Gly
NM_001354579.2:c.6122A>G	NP_001341508.1:p.Glu2041Gly