Canonical Allele Identifier: CA354805669

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142188965C>A (hg19) ; chr3:g.142470123C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470123C>A , CM000665.2:g.142470123C>A	GRCh38
NC_000003.11:g.142188965C>A , CM000665.1:g.142188965C>A	GRCh37
NC_000003.10:g.143671655C>A	NCBI36
NG_008951.1:g.113704G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6282G>T MANE Select	ENSP00000343741.4:p.Trp2094Cys
ENST00000513291.2:n.1466G>T
ENST00000654170.1:n.1125G>T
ENST00000656590.1:c.5072G>T
ENST00000661310.1:c.6090G>T	ENSP00000499589.1:p.Trp2030Cys
ENST00000665483.1:n.137G>T
ENST00000666447.1:n.117G>T
ENST00000666943.1:n.1746G>T
ENST00000350721.8:c.6282G>T	ENSP00000343741.4:p.Trp2094Cys
NM_001184.3:c.6282G>T	NP_001175.2:p.Trp2094Cys
XM_011512924.1:c.6288G>T	XP_011511226.1:p.Trp2096Cys
XM_011512925.1:c.6096G>T	XP_011511227.1:p.Trp2032Cys
XR_924147.1:n.6377G>T
XR_924148.1:n.6377G>T
XR_924149.1:n.6256G>T
NM_001354579.1:c.6090G>T	NP_001341508.1:p.Trp2030Cys
XR_001740179.2:n.6371G>T
XR_001740180.2:n.6425G>T
XR_001740181.2:n.6304G>T
XR_001740182.1:n.6256G>T
XR_002959543.1:n.6481G>T
XR_924148.2:n.6377G>T
NM_001184.4:c.6282G>T MANE Select	NP_001175.2:p.Trp2094Cys
NM_001354579.2:c.6090G>T	NP_001341508.1:p.Trp2030Cys