Canonical Allele Identifier: CA436125968

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142188968T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470126T>A , CM000665.2:g.142470126T>A	GRCh38
NC_000003.11:g.142188968T>A , CM000665.1:g.142188968T>A	GRCh37
NC_000003.10:g.143671658T>A	NCBI36
NG_008951.1:g.113701A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6279A>T MANE Select	ENSP00000343741.4:p.Leu2093=
ENST00000513291.2:n.1463A>T
ENST00000654170.1:n.1122A>T
ENST00000656590.1:c.5069A>T
ENST00000661310.1:c.6087A>T	ENSP00000499589.1:p.Leu2029=
ENST00000665483.1:n.134A>T
ENST00000666447.1:n.114A>T
ENST00000666943.1:n.1743A>T
ENST00000350721.8:c.6279A>T	ENSP00000343741.4:p.Leu2093=
NM_001184.3:c.6279A>T	NP_001175.2:p.Leu2093=
XM_011512924.1:c.6285A>T	XP_011511226.1:p.Leu2095=
XM_011512925.1:c.6093A>T	XP_011511227.1:p.Leu2031=
XR_924147.1:n.6374A>T
XR_924148.1:n.6374A>T
XR_924149.1:n.6253A>T
NM_001354579.1:c.6087A>T	NP_001341508.1:p.Leu2029=
XR_001740179.2:n.6368A>T
XR_001740180.2:n.6422A>T
XR_001740181.2:n.6301A>T
XR_001740182.1:n.6253A>T
XR_002959543.1:n.6478A>T
XR_924148.2:n.6374A>T
NM_001184.4:c.6279A>T MANE Select	NP_001175.2:p.Leu2093=
NM_001354579.2:c.6087A>T	NP_001341508.1:p.Leu2029=