Canonical Allele Identifier: CA436125959

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142188953A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470111A>C , CM000665.2:g.142470111A>C	GRCh38
NC_000003.11:g.142188953A>C , CM000665.1:g.142188953A>C	GRCh37
NC_000003.10:g.143671643A>C	NCBI36
NG_008951.1:g.113716T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6294T>G MANE Select	ENSP00000343741.4:p.Gly2098=
ENST00000513291.2:n.1478T>G
ENST00000654170.1:n.1137T>G
ENST00000656590.1:c.5084T>G
ENST00000661310.1:c.6102T>G	ENSP00000499589.1:p.Gly2034=
ENST00000665483.1:n.149T>G
ENST00000666447.1:n.129T>G
ENST00000666943.1:n.1758T>G
ENST00000350721.8:c.6294T>G	ENSP00000343741.4:p.Gly2098=
NM_001184.3:c.6294T>G	NP_001175.2:p.Gly2098=
XM_011512924.1:c.6300T>G	XP_011511226.1:p.Gly2100=
XM_011512925.1:c.6108T>G	XP_011511227.1:p.Gly2036=
XR_924147.1:n.6389T>G
XR_924148.1:n.6389T>G
XR_924149.1:n.6268T>G
NM_001354579.1:c.6102T>G	NP_001341508.1:p.Gly2034=
XR_001740179.2:n.6383T>G
XR_001740180.2:n.6437T>G
XR_001740181.2:n.6316T>G
XR_001740182.1:n.6268T>G
XR_002959543.1:n.6493T>G
XR_924148.2:n.6389T>G
NM_001184.4:c.6294T>G MANE Select	NP_001175.2:p.Gly2098=
NM_001354579.2:c.6102T>G	NP_001341508.1:p.Gly2034=