Canonical Allele Identifier: CA436125611

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142188191T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142469349T>G , CM000665.2:g.142469349T>G	GRCh38
NC_000003.11:g.142188191T>G , CM000665.1:g.142188191T>G	GRCh37
NC_000003.10:g.143670881T>G	NCBI36
NG_008951.1:g.114478A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6540A>C MANE Select	ENSP00000343741.4:p.Thr2180=
ENST00000513291.2:n.1724A>C
ENST00000654170.1:n.1383A>C
ENST00000656590.1:c.5330A>C
ENST00000661310.1:c.6348A>C	ENSP00000499589.1:p.Thr2116=
ENST00000665483.1:n.395A>C
ENST00000666447.1:n.375A>C
ENST00000666943.1:n.2004A>C
ENST00000350721.8:c.6540A>C	ENSP00000343741.4:p.Thr2180=
ENST00000513291.1:c.79A>C
NM_001184.3:c.6540A>C	NP_001175.2:p.Thr2180=
XM_011512924.1:c.6546A>C	XP_011511226.1:p.Thr2182=
XM_011512925.1:c.6354A>C	XP_011511227.1:p.Thr2118=
XR_924147.1:n.6635A>C
XR_924148.1:n.6635A>C
XR_924149.1:n.6514A>C
NM_001354579.1:c.6348A>C	NP_001341508.1:p.Thr2116=
XR_001740179.2:n.6629A>C
XR_924148.2:n.6635A>C
NM_001184.4:c.6540A>C MANE Select	NP_001175.2:p.Thr2180=
NM_001354579.2:c.6348A>C	NP_001341508.1:p.Thr2116=