Canonical Allele Identifier: CA436125989

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142189004C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470162C>T , CM000665.2:g.142470162C>T	GRCh38
NC_000003.11:g.142189004C>T , CM000665.1:g.142189004C>T	GRCh37
NC_000003.10:g.143671694C>T	NCBI36
NG_008951.1:g.113665G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6243G>A MANE Select	ENSP00000343741.4:p.Gln2081=
ENST00000513291.2:n.1427G>A
ENST00000654170.1:n.1086G>A
ENST00000656590.1:c.5033G>A
ENST00000661310.1:c.6051G>A	ENSP00000499589.1:p.Gln2017=
ENST00000665483.1:n.98G>A
ENST00000666447.1:n.78G>A
ENST00000666943.1:n.1707G>A
ENST00000350721.8:c.6243G>A	ENSP00000343741.4:p.Gln2081=
NM_001184.3:c.6243G>A	NP_001175.2:p.Gln2081=
XM_011512924.1:c.6249G>A	XP_011511226.1:p.Gln2083=
XM_011512925.1:c.6057G>A	XP_011511227.1:p.Gln2019=
XR_924147.1:n.6338G>A
XR_924148.1:n.6338G>A
XR_924149.1:n.6217G>A
NM_001354579.1:c.6051G>A	NP_001341508.1:p.Gln2017=
XR_001740179.2:n.6332G>A
XR_001740180.2:n.6386G>A
XR_001740181.2:n.6265G>A
XR_001740182.1:n.6217G>A
XR_002959543.1:n.6442G>A
XR_924148.2:n.6338G>A
NM_001184.4:c.6243G>A MANE Select	NP_001175.2:p.Gln2081=
NM_001354579.2:c.6051G>A	NP_001341508.1:p.Gln2017=