Canonical Allele Identifier: CA354793994

Gene: ATR

Linked Data

• dbSNP Id: rs2108242729
• MyVariant Identifiers: chr3:g.142168444C>T (hg19) ; chr3:g.142449602C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142449602C>T , CM000665.2:g.142449602C>T	GRCh38
NC_000003.11:g.142168444C>T , CM000665.1:g.142168444C>T	GRCh37
NC_000003.10:g.143651134C>T	NCBI36
NG_008951.1:g.134225G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.7762G>A MANE Select	ENSP00000343741.4:p.Ala2588Thr
ENST00000513291.2:n.6471G>A
ENST00000653893.1:n.2620G>A
ENST00000654170.1:n.2605G>A
ENST00000656114.1:n.2848G>A
ENST00000656590.1:c.6689G>A
ENST00000658083.1:n.2942G>A
ENST00000661310.1:c.7570G>A	ENSP00000499589.1:p.Ala2524Thr
ENST00000665483.1:n.5302G>A
ENST00000666447.1:n.4265G>A
ENST00000666943.1:n.4494G>A
ENST00000350721.8:c.7762G>A	ENSP00000343741.4:p.Ala2588Thr
ENST00000504521.5:c.351G>A	ENSP00000422553.1:n.351G>A
ENST00000513291.1:c.4826G>A
ENST00000515810.1:c.188G>A	ENSP00000421870.1:n.188G>A
NM_001184.3:c.7762G>A	NP_001175.2:p.Ala2588Thr
XM_011512924.1:c.7768G>A	XP_011511226.1:p.Ala2590Thr
XM_011512925.1:c.7576G>A	XP_011511227.1:p.Ala2526Thr
XR_924147.1:n.10519G>A
XR_924148.1:n.7994G>A
NM_001354579.1:c.7570G>A	NP_001341508.1:p.Ala2524Thr
XR_001740179.2:n.7988G>A
XR_924148.2:n.7994G>A
NM_001184.4:c.7762G>A MANE Select	NP_001175.2:p.Ala2588Thr
NM_001354579.2:c.7570G>A	NP_001341508.1:p.Ala2524Thr