Canonical Allele Identifier: CA354793943

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142168422A>T (hg19) ; chr3:g.142449580A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142449580A>T , CM000665.2:g.142449580A>T	GRCh38
NC_000003.11:g.142168422A>T , CM000665.1:g.142168422A>T	GRCh37
NC_000003.10:g.143651112A>T	NCBI36
NG_008951.1:g.134247T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.7784T>A MANE Select	ENSP00000343741.4:p.Ile2595Asn
ENST00000513291.2:n.6493T>A
ENST00000653893.1:n.2642T>A
ENST00000654170.1:n.2627T>A
ENST00000656114.1:n.2870T>A
ENST00000656590.1:c.6711T>A
ENST00000658083.1:n.2964T>A
ENST00000661310.1:c.7592T>A	ENSP00000499589.1:p.Ile2531Asn
ENST00000665483.1:n.5324T>A
ENST00000666447.1:n.4287T>A
ENST00000666943.1:n.4516T>A
ENST00000350721.8:c.7784T>A	ENSP00000343741.4:p.Ile2595Asn
ENST00000504521.5:c.373T>A	ENSP00000422553.1:n.373T>A
ENST00000513291.1:c.4848T>A
ENST00000515810.1:c.210T>A	ENSP00000421870.1:n.210T>A
NM_001184.3:c.7784T>A	NP_001175.2:p.Ile2595Asn
XM_011512924.1:c.7790T>A	XP_011511226.1:p.Ile2597Asn
XM_011512925.1:c.7598T>A	XP_011511227.1:p.Ile2533Asn
XR_924147.1:n.10541T>A
XR_924148.1:n.8016T>A
NM_001354579.1:c.7592T>A	NP_001341508.1:p.Ile2531Asn
XR_001740179.2:n.8010T>A
XR_924148.2:n.8016T>A
NM_001184.4:c.7784T>A MANE Select	NP_001175.2:p.Ile2595Asn
NM_001354579.2:c.7592T>A	NP_001341508.1:p.Ile2531Asn