Canonical Allele Identifier: CA436125979

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142188983T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470141T>A , CM000665.2:g.142470141T>A	GRCh38
NC_000003.11:g.142188983T>A , CM000665.1:g.142188983T>A	GRCh37
NC_000003.10:g.143671673T>A	NCBI36
NG_008951.1:g.113686A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000350721.9:c.6264A>T MANE Select	ENSP00000343741.4:p.Pro2088=
ENST00000513291.2:n.1448A>T
ENST00000654170.1:n.1107A>T
ENST00000656590.1:c.5054A>T
ENST00000661310.1:c.6072A>T	ENSP00000499589.1:p.Pro2024=
ENST00000665483.1:n.119A>T
ENST00000666447.1:n.99A>T
ENST00000666943.1:n.1728A>T
ENST00000350721.8:c.6264A>T	ENSP00000343741.4:p.Pro2088=
NM_001184.3:c.6264A>T	NP_001175.2:p.Pro2088=
XM_011512924.1:c.6270A>T	XP_011511226.1:p.Pro2090=
XM_011512925.1:c.6078A>T	XP_011511227.1:p.Pro2026=
XR_924147.1:n.6359A>T
XR_924148.1:n.6359A>T
XR_924149.1:n.6238A>T
NM_001354579.1:c.6072A>T	NP_001341508.1:p.Pro2024=
XR_001740179.2:n.6353A>T
XR_001740180.2:n.6407A>T
XR_001740181.2:n.6286A>T
XR_001740182.1:n.6238A>T
XR_002959543.1:n.6463A>T
XR_924148.2:n.6359A>T
NM_001184.4:c.6264A>T MANE Select	NP_001175.2:p.Pro2088=
NM_001354579.2:c.6072A>T	NP_001341508.1:p.Pro2024=