Canonical Allele Identifier: CA436107250

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142168412T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142449570T>G , CM000665.2:g.142449570T>G	GRCh38
NC_000003.11:g.142168412T>G , CM000665.1:g.142168412T>G	GRCh37
NC_000003.10:g.143651102T>G	NCBI36
NG_008951.1:g.134257A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.7794A>C MANE Select	ENSP00000343741.4:p.Arg2598=
ENST00000513291.2:n.6503A>C
ENST00000653893.1:n.2652A>C
ENST00000654170.1:n.2637A>C
ENST00000656114.1:n.2880A>C
ENST00000656590.1:c.6721A>C
ENST00000658083.1:n.2974A>C
ENST00000661310.1:c.7602A>C	ENSP00000499589.1:p.Arg2534=
ENST00000665483.1:n.5334A>C
ENST00000666447.1:n.4297A>C
ENST00000666943.1:n.4526A>C
ENST00000350721.8:c.7794A>C	ENSP00000343741.4:p.Arg2598=
ENST00000504521.5:c.383A>C	ENSP00000422553.1:n.383A>C
ENST00000513291.1:c.4858A>C
ENST00000515810.1:c.220A>C	ENSP00000421870.1:n.220A>C
NM_001184.3:c.7794A>C	NP_001175.2:p.Arg2598=
XM_011512924.1:c.7800A>C	XP_011511226.1:p.Arg2600=
XM_011512925.1:c.7608A>C	XP_011511227.1:p.Arg2536=
XR_924147.1:n.10551A>C
XR_924148.1:n.8026A>C
NM_001354579.1:c.7602A>C	NP_001341508.1:p.Arg2534=
XR_001740179.2:n.8020A>C
XR_924148.2:n.8026A>C
NM_001184.4:c.7794A>C MANE Select	NP_001175.2:p.Arg2598=
NM_001354579.2:c.7602A>C	NP_001341508.1:p.Arg2534=