Canonical Allele Identifier: CA354796780

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142232369C>G (hg19) ; chr3:g.142513527C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142513527C>G , CM000665.2:g.142513527C>G	GRCh38
NC_000003.11:g.142232369C>G , CM000665.1:g.142232369C>G	GRCh37
NC_000003.10:g.143715059C>G	NCBI36
NG_008951.1:g.70300G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.4615G>C MANE Select	ENSP00000343741.4:p.Gly1539Arg
ENST00000653868.1:n.4644G>C
ENST00000656590.1:c.3405G>C
ENST00000661310.1:c.4423G>C	ENSP00000499589.1:p.Gly1475Arg
ENST00000666943.1:n.79G>C
ENST00000350721.8:c.4615G>C	ENSP00000343741.4:p.Gly1539Arg
NM_001184.3:c.4615G>C	NP_001175.2:p.Gly1539Arg
XM_011512924.1:c.4621G>C	XP_011511226.1:p.Gly1541Arg
XM_011512925.1:c.4429G>C	XP_011511227.1:p.Gly1477Arg
XM_011512926.1:c.4621G>C	XP_011511228.1:p.Gly1541Arg
XM_011512927.1:c.4621G>C	XP_011511229.1:p.Gly1541Arg
XR_924147.1:n.4710G>C
XR_924148.1:n.4710G>C
XR_924149.1:n.4710G>C
NM_001354579.1:c.4423G>C	NP_001341508.1:p.Gly1475Arg
XR_001740179.2:n.4704G>C
XR_001740180.2:n.4710G>C
XR_001740181.2:n.4710G>C
XR_001740182.1:n.4710G>C
XR_002959543.1:n.4710G>C
XR_924148.2:n.4710G>C
NM_001184.4:c.4615G>C MANE Select	NP_001175.2:p.Gly1539Arg
NM_001354579.2:c.4423G>C	NP_001341508.1:p.Gly1475Arg