Canonical Allele Identifier: CA354814696

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142272179T>A (hg19) ; chr3:g.142553337T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142553337T>A , CM000665.2:g.142553337T>A	GRCh38
NC_000003.11:g.142272179T>A , CM000665.1:g.142272179T>A	GRCh37
NC_000003.10:g.143754869T>A	NCBI36
NG_008951.1:g.30490A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.2695A>T MANE Select	ENSP00000343741.4:p.Lys899Ter
ENST00000515149.3:c.*1469A>T	ENSP00000425897.3:n.*1469A>T
ENST00000653868.1:n.2724A>T
ENST00000656590.1:c.1485A>T
ENST00000659195.1:n.5570A>T
ENST00000661310.1:c.2503A>T	ENSP00000499589.1:p.Lys835Ter
ENST00000350721.8:c.2695A>T	ENSP00000343741.4:p.Lys899Ter
NM_001184.3:c.2695A>T	NP_001175.2:p.Lys899Ter
XM_011512924.1:c.2695A>T	XP_011511226.1:p.Lys899Ter
XM_011512925.1:c.2503A>T	XP_011511227.1:p.Lys835Ter
XM_011512926.1:c.2695A>T	XP_011511228.1:p.Lys899Ter
XM_011512927.1:c.2695A>T	XP_011511229.1:p.Lys899Ter
XR_924147.1:n.2784A>T
XR_924148.1:n.2784A>T
XR_924149.1:n.2784A>T
NM_001354579.1:c.2503A>T	NP_001341508.1:p.Lys835Ter
XR_001740179.2:n.2784A>T
XR_001740180.2:n.2784A>T
XR_001740181.2:n.2784A>T
XR_001740182.1:n.2784A>T
XR_002959543.1:n.2784A>T
XR_924148.2:n.2784A>T
NM_001184.4:c.2695A>T MANE Select	NP_001175.2:p.Lys899Ter
NM_001354579.2:c.2503A>T	NP_001341508.1:p.Lys835Ter