Canonical Allele Identifier: CA354805675

Gene: ATR

Linked Data

• gnomAD v4: 3-142470124-C-T
• MyVariant Identifiers: chr3:g.142188966C>T (hg19) ; chr3:g.142470124C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470124C>T , CM000665.2:g.142470124C>T	GRCh38
NC_000003.11:g.142188966C>T , CM000665.1:g.142188966C>T	GRCh37
NC_000003.10:g.143671656C>T	NCBI36
NG_008951.1:g.113703G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6281G>A MANE Select	ENSP00000343741.4:p.Trp2094Ter
ENST00000513291.2:n.1465G>A
ENST00000654170.1:n.1124G>A
ENST00000656590.1:c.5071G>A
ENST00000661310.1:c.6089G>A	ENSP00000499589.1:p.Trp2030Ter
ENST00000665483.1:n.136G>A
ENST00000666447.1:n.116G>A
ENST00000666943.1:n.1745G>A
ENST00000350721.8:c.6281G>A	ENSP00000343741.4:p.Trp2094Ter
NM_001184.3:c.6281G>A	NP_001175.2:p.Trp2094Ter
XM_011512924.1:c.6287G>A	XP_011511226.1:p.Trp2096Ter
XM_011512925.1:c.6095G>A	XP_011511227.1:p.Trp2032Ter
XR_924147.1:n.6376G>A
XR_924148.1:n.6376G>A
XR_924149.1:n.6255G>A
NM_001354579.1:c.6089G>A	NP_001341508.1:p.Trp2030Ter
XR_001740179.2:n.6370G>A
XR_001740180.2:n.6424G>A
XR_001740181.2:n.6303G>A
XR_001740182.1:n.6255G>A
XR_002959543.1:n.6480G>A
XR_924148.2:n.6376G>A
NM_001184.4:c.6281G>A MANE Select	NP_001175.2:p.Trp2094Ter
NM_001354579.2:c.6089G>A	NP_001341508.1:p.Trp2030Ter